Survey
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
University of Nigeria Virtual Library Serial No Author 1 ISBN 978 156 198 X NWADINIGWE, C A Author 2 Author 3 Title Inorganic Chemistry: A Guide to IUPAC Nomenclature (for Schools and Colleges) Keywords Description Inorganic Chemistry: A Guide to IUPAC Nomenclature (for Schools and Colleges) Category Physical Sciences Publisher Fourth Dimension Publishers Publication Date Signature 1985 INORGANIC CHEMISTRY: A GUIDE TO IUPAC NOMENCLATURE (FOR SCHOOLS AND COLLEGES) INORGANIC CHEMISTRY: A GUIDE TO IUPAC NOMENCLATURE (FOR SCHOOLS AND COLLEGES) INORGANIC CHEMISTRY: A GUIDE TO IUPAC NOMENCLATURE (FOR SCHOOLS AND COLLEGES) by C. A. NWADINIGWE F[3P FDURTH OIMENS(0N WELISHEAS First Publsihed 1985 by Fourth Dimension Publishing Co., Ltd. 64A City Layout, P.M.B.1164 Enugu, Nigeria 0 1985 by C.A. Nwadinigwe ISBN 978 156 198 X CONDITIONS All rights resenred. No parts of this publication may be reproduced, stored in a retrieval system, or transmitted in any form or any means, electronic, mechanical, photocopying, recording, or otherwise without the prior permission of the Publisher. Photoset and printed in Taiwan, R.O.C. by At-UNITED INDUSTRIES & SHIPPING INC. 10th FI., Cheng Chung Great Building No. 12-1, Lane 5, Lin Shen North Road Taipei, Taiwan CONTENTS 1 NAMES AND SYMBOLS OF THE ELEMENTS ......... 2 INDICATlON OF MASS. CHARGE. ETC., ON A'TOMIC SYMBOLS ............................................... 3 THE USE OF ARABIC NUMBERS. ROMAN NUMERALS. AND GREEK I'REFIXES .................... 4 OXIDATION NUMBER CONCEPT .......................... 5 NOMENCLATURE WlTH RESPECI' TO IONS ......... (i) cations ................................ (ii) anions ............................................................ ....................... . 6 NOMENCLATURE WITH RESPECT TO ACIDS ....... (i) two element acids .....,.. ................................. ................... ................................ .............. ................................... 7 NOMENCLATURE WITH RESPECT TO BASES ....... (i) amphoteric oxides ........................................... (ii) basic oxides (iii) hydroxides ..................................................... .................................................... WITH RESPECT TO SALTS ....... (i) simple (anhydrous) Qlts ................................... (ii) acidic salts ..................................................... ( i i i ) basic salts ...................................................... (iv) salts with water of crystallkation ........................ 8 NOMENCLATURE 9 DOUBLE SALTS. GUIDELINES FOR FORMULAE AND NOMENCLATURE ........................ ............ .. 10 THE HALIDES OF CARBON. C X , .......................... 1 1 FREE RADICALS ................................................ 12 FORMULAE AND NAMES OF COMPOUNDS IN GENERAL 29 13 FORMULAE AND NAMES OF SOME COMMON COMPOUNDS ................................. .................. 31 ............................................................. ... APPENDIXES 1. The periodic table of elements ................................. 2 . Oxidation states of elements in the periodic table .......... 3 . Table of elements. symbols. atomic number and relative atomic masses ....................................................... ................................................ 5 . Glossary ............................................................... 4 . Answers to questions 37 38 39 42 43 PREFACE Thc abbreviation IUPAC stands for the International Union of Pure rind Applied Chemistry, a body charged with the difficult task o f pronwtmg understanding among chemists all over the world. The Union has many Commissions under it, each Commission working on different topics in Chemistry. The Commission on the Nomenclature of Inorganic Chemistry of the IUPAC was formed in 1921. It drafted a ~t of rules which was published in 1940. This "1940 Rules" have been revised and rewritten severally in keeping with the Commission's aim of producing rules which lead to clear and acceptable names for as many inorganic compounds as possible. There are two essential requirements for the name of any chemical compound: (i) (ii) ~~ I I 1 it must be understood by other chemists, and it must designate the compound unambigously. To achieve these ends, it is desirable that all chemists should use the same rules of nomenclature. ThisA~bookhas become quite necessary as a result of the shift of emphas~sby the major examining body in West Africa, the West African Examinations Council, .from the traditional nomenclature to the IUPAC system. In the absence of any readily available reference b w k s on the subject, schools, colleges, and private candidates sitting for ordinary and advanced level examinations in chemistry have had teething problems adjusting to the new system. Most textbooks in inorganic chemistry are yet t o be revised to reflectathe new system of nomenclature. In the presentation, guidelines for naming the various types of ions and compounds encountered in 0-and A- level inorganic chemistry are given, in the hope that such guidelines will enable the user to name any compound not specifically mentioned in the book. Chemistry teachers will find this approach quite useful. T h e book will also satisfy the needs of Laboratory Chemical Suppliers, enabling them to use IUPAC names o n their labels and in their catalogues. University undergraduate students and other students in institutions of higher I learning who take first year inorganic chemistry courses will find the book a useful companion. I have consulted introduction to Chemical Nomenclature by R. S. Cahn and 0. C. Dermer, fifth edition, Butterworths, London 197'1; f U P A C Reports, J . Amer. Chem. Soc., 82, 5523 (1960); IUPAC, Nowrenclature of Inorganic Chemistry, second edition, Definitive ~ h e 1970, s Butterworths, London, and I am much indebted to them. The author wishes to thank Drs. A. Ahmed and F. Nwabue and Mrs. A . 0. Nwadinigwe, B.Sc., P.G.D,E., who read the work in typescript and advised 01 NAMES AND SYMBOLS OF ELEMENTS There are about 105 known elements. Their names and symbols form the basis of chemical names and formulae. The periodic table of clznlcnts found in many chemistry books is also constructed with these symbols. Such a table is given here in Appedix 1. The International Union of Pure and Applied Chemistry [TUPAC) has adopted the names and symbols given in Appendices 1and 3 for these elements, except for the last two. These two elements, with atomic numbers 104 and 105, were quite recently dihiovered and so official names or symbols have not yet been adopted for them. The following group names should be. noted in the periodic table: (i) all the group I elements are collectively called the ALKALI metals, (ii) all the group V11 clc~~rcntsurc collcctivcly cullcd tile HALOGENS, and (iii) all the group 0 elements are collectively called the NOBLE GASES. Isaddition, the lUPAC recommends that any new metallic olcnwnts discovered should be given names ending in -ium. This will then be consistent with the names of most of the already known nletals. Examples: aluminium, barium, beryllium, calcium, chromium, lithium, magnesiutn, etc. It also recommends that all new dements shall have two-letter symbols (like Al, Ba, Be, Ca, etc.) and that all the isotopes of an element should have the same name but differentiatedby the mass numbers. Example, the isotopes of oxygen are named oxygen-16,-oxygen-17, and oxygen-18. INDICATION OF MAS!!, CHARGE, ETC., ETC., ON ATOMIC SYMBOLS The symbol of an element, when fully and correctly written, provides the following information about the element: (i) its isotopic mass number (defined as the sum of the protons and neutrons in the atomic nucleus), (ii) its atomic number (defined as the number of protons in the atomic nucleus or the number of electrons in an electrically neutral atom), (iii) the charge on the ion, and (iv) the number of atoms of thc GICIIICIIL. T o convey these information, the notation recommended for writing the symbol of an element X, is: where the left upper index, a, represents the mass number, the left lower index, c, represents the atomic number, the right lower index, d, represents the number of atoms, and the right upper index, b, represents the ionic charge. illustrative examples: :tie represents an atom of helium of mass number = 4 and atomic number = 2. It must be noted that in the representawhile d (the tion :He, b(the ionic charge) is assumed to be 0, number of atoms) is assumed to be 1. In general, when no charge is given for b, it is assumed to be 0 charge (neutral) while in the case of d, if no number is given it is assumed to be 1. 0 represents a molecule of trioxygen (trivial name = ozone) containing 3 atoms, each of which has the atomic number = 8 and mass number P: 16. There is no ionic charge, i.e. the molecule is neutral. represents a molecule of oxygen (made up of 2 atoms). The isotopic mass number = 18 while the atomic number = 8. reprcscnts a molecule of chlorine (made up of 2 atoms). Thc isotopic mass number = 35 while the atomic numbcr = 17. represents one atom of sodium whose atomic number = 11 and the ionic charge = + 1. represents an isotope of sulphur atom. The mass numher = 34, the atomic number = 16, and the io~iiccharge = 'lie following points should be noted. Ionic charge should be indicated as Xn+and not as X+" Examples: ~ a ~ not + ,~ a + ~ 02-,not 0-' When a compound is isotopically labelled, the symbol of the isotope in parenthesis is added to the name of the compound. Examples: 3 2 ~ is~ phosphorus ~ 3 ( 3 2 ~ ) trichloride H ~ CisI hydrogen chloride ("Cl) " N H ~is ammonia (I5N). For allotropes, the systematic names are based on the size ~nolccule.The size is indicated by Greek numerical prelixes. When the number of atoms is large and unknown. the prefix "poly" is used. For ring and chain structures prefixes "cyclo" and "catena" respectivcly are used. Symbol H Trivial name atomic hydrogen Systematic name monohydrogen 0 2 dioxygen triox ygen S8 oxygen o-zone white phosphorus (yellow phosphorus) A-sulphur s,, p-sulphur 0 3 p4 tetraphosphorus cy clooctasulphur or octasulphur catenapolysulphur or polysulphur Questiurts: . :s2- Explain the difference between lMOzand 02, and ::S, ?$I and ::cI,,;ECa and :dCa2+, f H and :H,. 2. If a potassium nuclide has atomic number = 19, mass number = 39 and ionic charge = 1+, represent this atom sy~nbdicully. 1. THE USE OF ARABIC NUMBERS, ROMAN NUMERALS, AND GREEK PREFIXES numeral Roman numeral equivalent I I1 I11 IV v VI VII VIl I IX X XI XI1 Greek numerical prefix equivalent mono di t rib tetra penta hexa hepta octa nona deca undeca dodeca The prefix "mono" may generally be omitted. Beyond 12, Greek p r e f i s s are sometimes replaced by Arabic uumcrals because they are more readily understood. The Arabic numbers are used when writing molecular formulae: to indicate the number of atoms of a particular elemcnt prcscnt in a molecule. E.g. H 2 0 . Here 2 shows that there are 2 hydrogen atoms in a molccule of water. Similarly ill SO,, H2S03, and PbSO,, the numbers 2, 3, and 4 show there are respectively 2, 3, and 4 oxygen atoms in a molecule of SO,, H z S 0 3 , and PbSO,. (ii) tb indicate the number of moles of i~ compound. Examples: 2H20, 3S02, 4H2S0.3and 5PbS04 suggest 2, 3,4 and 5 moles respectively of HzO, SO2, I-12S03 and PbSOJ. (iii) to indicate the number of times a group which is cnclosrtl in parenthesis occurs. Examplc: (NI-l,)2S04, Pb(N03)-,, Fe2(S0,), indicate that the groups N H 4 , NO3, and SO4, occur 2, 2, and 3 timcs respectively in a n~oleculeof (NH4j2SO4, Pb(N03)?, and Fe2(S04)3. (iv) to indicate the number of watcr of crystallization and similar loosely bound muleculcs. (i) Exumples: in in in in CuS04.5H20, IIuIIIVLL w(llL1of crystallization is 5 FeS04 .7H,O, the number of water of crystallization is 7 MgS0,.7H20, the number of water of crystallization is 7 Na2C03. 1 0 H 2 0 , the number of water of crystallization is 10 LIIL The Roman figure is very often used to indicate the oxidation state oI the key atom in a molecule or.ion especially if that key atom can have variable oxidation states. Examples: FeCI, = iron FeC13 = iron FeO = iron Fe203= iron (11) chloride (111) chloride (11) oxide (111) oxide N 2 0 = nitrogen (I) oxide N O = nitrogen (11) oxide NO2 = nitrogen (IV) oxide NO3 = nitrogen (VI) oxide O n the other hand, the Greek prefix can be encountered in a number of situation, including: (i) indicating the number of ligands in parenthesis. e.g. K4Fe (CN), = potassium hcxacyanoferrate (11) (ii) indicating the number of oxygen atoms in an anion: e.g. SO:- = tetraoxosulphate (Vl) ion SO$- = trioxosulphak (IV) ion (iii) indicating the number of water of crystallization e.g. FeS0,.7Hz0 = Iron (11) tetraoxosulphate (VI) heptuhydrate. THE OXIDATION NUMbER CONCEPT rile IUPAC nomenclature makes immense use of the crxidation number of atoms in a molecule. The oxidation number should be specified for: , -- -tals and non-metals that can have variable oxidation states rnples: CuzO = copper (I) oxide. Here (I) refers to the 3ation number of the copper atom. C O = carbon (11) oxide. : (11) refers t o the oxidation number of carbon. key o r central atom in the anion of a salt if that anion - - ~ a i n smore than one element, e.g. SO:-, tetraoxosulphate (VI) ion, here (VI) refers to the oxidation state of the sulphur .om. le key atom in the anion of an acid if that anion contains more Ian one element. \ It is, therefore, quite useful to be able to determine the oxidation number of any atom in a molecule. We can introduce the concept of oxidation number by considering these three reactions: br (i) Na (s) + 3Fz (s) ---, NaF (s) (ii) 3Fz (g) + 4F&) ---* F2 (d (iii) iH2 (d + -9Ch (g) HCl (g) ftcaction (i) can be represented as: - nuclcuh (I!!', l 2 N ) nucleus ( W . ION) ':F nuclcus (Ill'. 12N) + ~~uclcu~ (sf', ION) I I N a ( 1 0 electrons) ,F-(10 electrons) In the above illustration, the sodium atom is oxidised (by complete transfer of one electron, the valence electron) to become the sodium ion. T h e sodium ion has one positive charge (since it now has 10 electrons and 11 protons). Consequently, sodium is said to have an oxidation number of +l. The fluorine atom which accepts the one dectron from sodium to complete its octet now has a net -1 charge, with 9 protons against 10 electrons. Consequently fluorine atom has a - 1 oxidation number. In t h ~ example, s there is a complete transfer of electron from one atom t o the other because the fluorine atom has a much greater affinity, a much greater propensity for electrons. O r , t o use the chemist's language, the fluorine atom is muchlmore electronegative than the d i u m atom. In the second reaction, i,e. (ii), the two fluorine atoms are of equal electronegativity and so an electron cannot be transferred from w e atom to the other. The resulting fluorine molecule is formed by sharing two electrons equally between the two atoms, resulting in a nonpolar covalent bond:, nucleus (YP, 10N) nucleus (W. IUN) Using the electron-dot notation this can be represented as: 'Therefore, in the fluorine molecule one can still picture each atorrl as consisting of 9 positive charges and 9 negative charges (9 protons and 9 electrons), giving a net zero charge. T h e oxidation number of Huorine in F2 is then equal to 0.The same deduction holds for any free element such as hydrogen in Hz,chlorine in C12, sodium in Na, oxygen in 02,sulphur in S,, phosphorus in P4,etc. . In the third reaction, i.e. reaction (iii), because c h l o r i r is only slightly more electronegative than hydrogen it does not involve a complete transfer of electrons from hydrogen to chlorine and it does not involve an equal sharing of electrons as in (ii). The electrons are regarded as displaced towards the more electroneyative chlorine atom, giving rise to a partial covalent bond. ':cl t ICI r the purpose of oxidation number calculations, the ulsplactru c l c ~ ~ l o are ns counted with the more electronegative atom. I n this case the chlorinc atom will appear to have a -1 charge and the hydrogen atom will appear to have a +1 charge. Thii gives the oxidation number of hydrogen and chlorine in HCI as +1 and -1 respectively. The deductions are also general for other partial covalent bonds, namely: the displaced electrons are counted with the more electronqptive atom. ridation number then refers to the charge which an atom in a ~olecu& would hove if the bonding electrons were a s s i p w i arbitrarily lu the more electronegative element. Rules for w i p i n g oxidation numbers In principle, electronic ,pictures a s illustrated in (i), (ii) and (iii) above can be drawn for any molecule and the bonding electrons assigned arbitrarily to the more electronegative element. However, deciding oxidation numbers by this approach is quite laborious. In practice, oxidation numbers are ordinarily obtained in a much easier way by applying the following operational rules: 1. For free elements, each atom has an oxidation'number of 0,no matter how complicated the molecule is. Example, fluorine in F2, iodine in I,, hydrogen in Hz,phosphorus in P,, sulphur in Ss, sodium in Na, all have oxidation numbers = 0. 2. In ions which contain one atom (monoatomic ions), the oxidation number of the element is equal to the charge on that ion. + , CI-, s2-,02-,the oxidation Example, in ~ e ~~ +e ,~ K+, numbers of iron, potassium, chlorine, sulphur and oxygen are the charges on the respective ions, i.e. +2, +3, +1, -1, -2. -2 respectively. Consequently, in the ionic corlrpound NaCI, the oxidation number of sodium = 1 and the oxidation number of + chlorine = - 1. I t is helpful t o remember that the group I elements of the periodic table (Appendix 1) from only +1 ions. Their oxidation number is + 1 in all compounds. The group I1 elements form only +2 ions and so always have + 2 oxidation numbers in all compounds. 3. In most compounds containing oxygen, the oxidation number of the oxygen atom is -2. Example, in H 2 0 , SO2, CaO, etc, the oxidation number of the oxygen atom is -2. The only exception to this rule is inperoxides where the oxygen atoms have oxidatio'n number = -1. i.e., in H 2 0 2 , Na20z and other peroxides, the oxidation number of the oxygen atom = -1. 4. Hydrogen in its compounds ordinarily has an oxidation number of + l . Example: in H 2 0 , H2S, HF, H2SO4, etc, the oxidation nuniber of the hydrogen atom is + l . The only exception here is in metul hydrides (where hydrogen is the more electronegative atom). In metal hydrides, tne oxidation number of the hydrogen atom is - 1. i.e., in NaH, CaH2, ctc, the hydrogen atom has a -1 oxidation number. 5. All oxidation numbers must be consistent with the conservation of charge. This means that for: (a) neutral molecules (i.e., molecules without any charges), the oxidation numbers of all the atoms must add up to zero. (b) ions which contain more than one atom, the oxidation number of all the atoms niust be equal to the charge on the ion. The application of these rules is illustrated in the examples below: What is the oxidation number of sulphur in &SO4? Solution: + For H2S0,, knowing that the oxidation number of hydrogen is i (rule 4), that of oxygen is -2 (rule 3) and that the molecule is neutral, implying that the sum of all the oxidation numbers must be O (rulc 5a), we have: IizS04 i.e. - 2 (-1- 1) +2 + [oxid. .no. of + [oxid S ] t J( -2) = O =O =+X-2 no. of SJ - X oxid. no. of S = +6 mine the oxidation number of Mn in KMnO, .., XMn04, knowing that the oxidation number of potassium =. + I (rule 2), the oxidation number of oxygen = -2 (rule 3), and that the molecule is neutral, implying that the sum of all the oxidation numbers must = 0 (rule 5a) we have: KMnO, = +1 +I + [oxid. no. of Mn] + 4(-2) + [oxid. no. of Mn] - 8 oxid. no. of Mn =O 0 =+8= +7 =: 1 Calculate the oxidation number of nitrogen in NO;. For N O i , knowing that the oxidation number of oxygen = -2 (rule 3), and that the net charge on the ion is -1, implying that the sum of all the oxidation numbers nlust = - I (rule 5b), we haw.. NO; = [oxid. no. of N] i.e. or + 3(-2) [oxid. no. of N] -6 oxid. no. of N = = -1 -1 =-1+6 = +5 Show that the oxidation number of chromium in K,Cr,O, is 1-6. For K1Cr2O7. knowing that the oxidation number of poti~ssiu~n is t 1 (rule 2). that of oxygcu is -2 (rule 3) and that t l ~ cmolcoulc is ncutrai, i x . , the sum of all the oxidation nunlbers equals 0 (rule 5a). we have: K,Cr,O, i.e or = 2(+1) +2 + [oxirk + [oxid. no. of ZCr] no. of ZCr] oxid. no: of 2Cr + 7(-2) = O 14 = O = = +14 - 2 +12 +6 - from which oxid. no. of Cr = Questions: 3. Calculate the oxidation number of sulphur in the ion and compounds below: (i) so3 (ii) SO:-' (iii) Na2S203 4. What is the oxidation number of: (a) chlorine in each of the following compounds: NaCI, NaCIO, NaCI0.3, NaCI03? (b) manganese in each of the following compounds: Nu,MnO,, M n 0 2 , NaMn04 , Mn,O,, Mn207? chromium in the ions CrO;, Cr20;', 00:-,IiCrO, , (c) C ~ O H? ~ + 5. Give the oxidation number of each aton1 in: (a) As2U3 (b) C a C 2 0 4 (c) PFS (d) NO; ( e ) C r 2 0 ; - (f} 0; 6 . State the oxidation number (a) Pb in P ~ C I ~ (c) Re in ReO; ( e ) Bi in BiOi(g) M o in (~o,Cl,)'' of: (b) Sn in Sn2F; (d) Xe in HXeO; ( f ) N in (NH,OH)+ (h) in (H~W1204u)6- 7. Calculate the change in oxidation number of the underlined atoms in the reactants and products of the following equations: (i) 2K2-Cr,O, (s) + 2 H 2 0 + 3s (s) 3 S o 2 (g) + 4KOH (s) + 2Cr-20, 2KCl (s) + 30.-2 (g) (ii) 2KClO-, (s) - + 8. Consider the q u a t i o n : 2Mn0, (aq) + 10 Cl- (aq) + 16H' - (aq) 2Mn2+ (aq) + 5Ci2 (g) + 3H20 Find the oxidation number of each clement on both sidcs of the a,...-t.n- charged species. Two main types are known: cations and anlorn. (i) Cations: &tions are ions that carry positive charges. In inorganic nornenclaturc the two common types are cations with variable oxidation numbers and those with fixed oxidation numbers. In earlier nomenclatures, variublc oxidation states were clislinguished by means of suffixes, -ous and -ic, added to the root of the name of the cation. e.g. plumbous ....... plumbic cupprous ....... cuppric ferrous ....... ferric The IUPAC recommends that the use of this type of no~~icnclature may be' retained only for elements exhibiting not more than two valences. A more favoured no~ncnclatureis that the ionic symbols of nlonoatonlic cations are named like the correspondirig element, with%t change or suffix, while thosc with variablo oxidation states are named by Srock's sysrcrn, that is, they have the appropriate oxidation numbers written in Ron~iinnun~crals,c~icloscdin parcnthesis, and placed immediately after the nnn'e of the catio~i. (a) Fixed oxidation state: Li lithium ion Na+ sodium ion MgZ+ magnesium ion Ca2' calcium ion NHZ ammonium + (b) Variable oxidation states: Fez+ iron (11) ion Fe" iron (111) ion Cu+ copper (I) ion Cu2+ copper (11) ion PbC12 lead (11) chloride Polyutornic cutions: When a polyatomic cation is formecI trom a monoatomic cation by the addition of other ions o r neutral atoms or molecules (ligancis), that polyatomic cation will be regarded as a complex and will be named according.to the rules'of coordination nomenclature. ' [A1 (H~o),]'' = the h e m aquoalurninium (111) ion [CoCI (NN,)~]~ = the chloropent;~mminecobalt (Ill) ion Cations from nitrogen buses The cation formed by adding a proton to ammonia rtrtai~isthe fan~iliarname ammonium ion. Substituted ammonium ions have urnmonium as suffixes. Examples: NH,) ammonium ion HO-i~ hydroxylammoniurn , ion (CH,),NH (11) trimethylammonium ion FROM OTI-IER NITROGEN BASES: Cations from other nitrogen bases (e.g. pyridine , hydrazine, aniline) h a i e the ending "-ium" added to the name of the base (if necessary omitting a final -e o r other vovel in the name of the base). Examples: base Cation (pyridine) H+ H2N-NH, + (hydrazine) H2N-NH3 C,H,NH, (aniline) C,H$H (pyridinium ion) (hydrazinium ion) (anilinium ion) If a base can give more than one cation, thc appropriate charge is indicated in the names E.g. hydrazine hydrazinium (1 +) ion hydrazinium ( 2 + ) ion rr3v 15 a monohydrated proton and the recommended IUPAC name is oxo~liumion. Derivatives of this parent ion has "oxunium" occurring in their names. CH30ki: methyloxonium ion (CH,),OH+ dimethyloxoniurn ion H 3 0 'CIO; oxonium perchlorate Curions from acids: When cations are formed by adding protons to acids, their names are formed by adding the word "acidium" the name of the corresponding anion. r) Exurrrplrs: H2N0,' H2N0; CH,COOH+ (ii) = = = the nitrate acidium ion the nitrite acidium ion the acetate acidium ion Anions: These arc atoms o r groups of atoms which are negatively The following guidelines are useful in naming anions: (a) In general, the names of monatomic anions end in "-ide." Thus, HDFC1- = hydride ion deuteride ion = fluroide ion = chloride ion Br- = bromide ion I - = iodide ion 0'- = oxide ion s'- = sulphide ion = = selenide ion = telluride ion = = = = = = nitride ion phosphide ion arsenide ion antinionide ion carbide ion boride ion (b) The names of polyajomic anions consist of the name of the central atom with the ending "-are". E.g., NO, [lSb(OH),] (c) = trioxonitrate (v) ion = hexahydroxoantimoncrrp (v) ion A few polyatomic anions have names ending in "-idc". These are to be regarded as exceptions to the rule. E.g. OH - = hydroxide ion 0;peroxide ion 02 hyperoxideion 0, ozonide ion S: disulphide ion 1; triiodidt: ion HF; hydrogen difluor~deion. (d) NNH*~ NH; NHOHN21-Ii CN- c;- azide ion imide ion amide ion hydroxylamide ion hydrazide ion cyanidc ion acetylide ion Some anions have their names ending in thc letter "o". This obtains when such anions occur in complex compounds o r when they are used in combination with other anions in the same molecule. Under these situations we have,. for example: 02 - -- OX0 OH-- = hydroxo CN- = cyano (e) The 0 x 0 crniotu: Some anions such as NO3, SO:-. YO:,etc, retain the tamiliar endings nitrate, sulphate, and phosphate respectively. However, the oxidation number of the central atom is specified in Roman nunwrals and the number of oxygen atoms (0x0 atoms) present indicated by Greek prefixes. The following examples are illustrative of this new system: - = ctioxonitrute (HI) ion trioxonitrate (V) ion = trioxosulphate (1V) ion = tetraoxosulphate (VI) ion (VI) ion = tetraoxophosphate (V) ion = trioxocarbunate (IV) ion = tetraoxophospliatc - = heptaoxodichromate ( V l ) ion rnonoxochlorate ( I ) ion rioxochlorate (V) ion etraoxomanganate (VII) ion lydrogen tetraoxosulphate (VI) ion ~ydrogentrioxocarbonate (IV) ion trioxosulphursulpharc ( V I ) ion (one of [he sulphur arollls I S a ligilnd) iroxoperoxodisulpha~c(V1) ion :term pcroxo is uwd for -0-0-Imkayc) ACIDS NOMENCLATURE WITH RESPECT TO ACIDS Arrhenius (1887) defined an acid as e substance that can increase the concentration of H+ (actually H30+) ion in aqueous solution. E.g.9 HCl + H20 ---, H,O+ + C1Bronsted-Lowry defined an acid as a substance that can donate a proto11 to some other substances. E-g., H2S04 H+ + HSOi or H2SO4 2H+ -t- SO:- = (i) Two element acids: From these definitions, an acid has two portions; the catbn part which is H+ and the anion part (which carries the negative charge). In naming acids by the IUPAC recommendation, the following guidelines are helpful: (i) For aclds that contain only two elements, the general rule applies, namely: the name of two element cornpounds end in "-id&'. Examples: HCI = hydrogen chloride acid HP = hydrogen fluoride acid HBr = hydrogen bromide acid I = hydrogen iodide acid ' (ii) 0 x 0 acids: For the 0x0 acids, the anion part is named accordingly (as illustrated -under anions) but the word "acid" is added in place of "ion". Exumples: I UPAC name dioxonitrate (111) acid zrioxonitrate (V) acid trioxosulplial tetraoxosulpl trioxocarbon tetraoxophos tetraoxophos (iii) Acidic oxides: Elements on the right of the periodic table do not form simple ionic oxides. They share electrons with oxygen atoms. Many of these molecular oxides, such as sulphur (IV) oxide, SO2, an= gases at room temperature and dissolve in water to give acidic solutions. Exumples: SO, (g) + H,O CO, (g) + HzO SO, (g) t H 2 0 j)I+ + HSO; + CO$~ ++SO:- 2H' 2 The molecular oxides are, therefore, called acidic oxides or acidic anhydrides. In their nomenclature by the IUPAC recommendation the naBes end in "-iden since they are two element compounds. The oxidation number of the key atom is also given in parenthesis. Exumples: SO, SO, NO N20 sulphur (IV) oxide sulphur (VI) oxide nitrogen (11) oxide nitrogen (I) oxide NO3 Si02 C02 CO nitrogen (VI) oxide silicon (IV) oxide carbon (1V)'oxide carbon (11) oxide However, there are compounds which cannot be named easily and unambiguously by the above method which is known as the Stock System. For example, the name nitrogen (IV) oxide describes both NOz and N204. In such situations the use of Greek numerical prefixes is preferred: NO, N204 P205 P40,, nitrogen dioxide dinitrogen tetroxide diphosphorus pentoxide tetraphosphorus decoxide NOMENCUTURE WITH RESPECT TO BASIC OXlDFS A N D BASES (i) Amphottric oxides: It is not possi.ble to classify all known oxides sharply as either acidic or basic. Some oxides, especially those formed by elements towards the centre of the periodic table are intermediate in behaviour. They are able to neutralise both acids and bases. They are known as amplwteric oyides. E.g., ZnO ZnO (s) ZnO (s) -- + 2H+ ZnZ+ + + 2 0 ~ - & +H 2 0 HZO [Zn (OH)$- However, it is quite straight-forward naming these oxides. Most of them are compounds with only two different types of atoms. Cunsequently, their names end in "-ide",, Examples: ZnO AI2O3 Sb203 As203 = zinc oxide = aluminium (111) = antimony (111) OAIUG = arsenic (111) oxide (ii) Basic oxides: These are also binary compouncIs and so their names end in "-id&'. 10s. Na,O LizO CaO sodium oxide; lithium oxide; calcium oxide; CuO copper (11) oxidc MgO magnesium oxide BaO barium oxide (iii) Hydroxides: Hydrogen are three or more element compounds. We will, therefore, expcct their names to end in "-aten. This does not obtain and all hydroxides, whether basic or ampboteric have their names ending in .'-ide" like two dement compounds. They nnay be regarded as exceptions t o therule. N o Roman figures are netcessary except where the metal atom can exhibit variable oxidation sta tes. The metal or the more electropositive component is named ti1rst followed by the "hydroxide" ending. KOH potassium hydroxide Mg(OH)2 magnesium hydroxide AI(OH), aluminium hydroxide Fe(OH)2 iron (11) hydroxide Fe(OH)3 iron (111) hydroxide Ca(OH), calcium hydroxide Cu(OH), copper (11) hydroxide NaOH sodium hydroxide Zn(OH)* zinc hydroxide NOMENCLATURE WITH RJISPECT TO SALTS (i) Simple (anhydrous) salts. Simple salts are derived from acids by neutralization reactions with bases: Base + Acid = Salt + NaOH + HCI = NaCl + Ca(OH)i+ H2S04 = CaS04 N H 4 0 H + HN03 =. NH4NOJ + water H20 + 2H20 H20 The formation of a salt can then be looked upon as the replacement of the hydrogen ion(s) in the acid by a metal or electropositive group. In the IUPAC nomenclature, the name of this metal or electropositive group is added to the name of the anion component of the acid from which it is derived. If the metal can have variable oxidation numbers, the appropriate one is indicated in Roman numeral enclosed in parenthesis ( ) and placed immediately after the name of the metal. The oxidation state of the central atom in the anion portion is also indicated in Roman numerals as the examples below illustrate: Kl NaCl CaSO, FcS04 Fe2(S04), Na2C03 CuSO, NH4N02 NH,N03 CaC03 PbS03 NaOCl NaCIOJ = potassium iodide = sodium chloride = calcium tetraoxosulphate (VI) = iron (11) tetraoxosulphate (VI) = iron (1li)tetraoxosulphate (VI) = sodium trioxocarbonate (1V) = copper (11) tetraoxosulphate (VI) = ammonium dioxonitrate (111) = ammonium trioxonitrate (V) (IV) (IV) = sodium monoxochlorate (I) = calcium trioxocarbonate = lead (11) trioxosulphate = sodium trioxochlorate (V) It must be noted thqt fractional oxidation ,numbers cannot be represented in Roman numerals. E.g., the oxidation number of silver in AgzFis + 4. In naming such compounds withI fracticnnl nv;rl..t;-V ~ I U U L I U I I numbers, the use of Greek numerical prefixes is pre f a r e d . Thus, Ag2F is disilver monofluride. ,119. (ii) Acidic salts: Their IUPAC names end in "-atew because th ey contam more than two different atoms per molecule. The metal is 1named first, followed by the hydrogen, and the anion group is name(d last. The oxidation number of the key atom in the anion portionI is also indicated in Roman numerals: NaHS03 sodium hydrogen trioxosulphate (IV) NaHSOI sodium hydrogen tetraoxosulphate (VI) KHC03 ljotassium hydrogen trioxocarbona te (IV) (iii) Basic d t s : The cation is named first and then the other combining groups are named ikalphabetical order. Mg(0H)CI = magnesium chloride hydroxide (here chloride comes before hydroxide in keeping with the alphabetical order rule) CY~(OH)~CI = copper (11) chloride trihydroxklc (here again chloride comes before hydroxide in alphabetical order) tiv) SaIts with water of crystcrllization: In. general, water of crystallization and similar loosely bound molecules are designated by means of Arabic numerals before their The salt portion is named as explained formulae e.g., FeS04.7H20. above for simple salts. This is then followed by a description of the exact number of molecules of water associated with the salt. Any of three methods can be used to describe this water of crystallization: Na,C03. 10 H 2 0 = sodiuh trioxocarbonate (IV) decahydrate MgSOJ . 7 H 2 0 = magnesium tetraoxosulphate PI)heptahydrate FeS0, .7HZ0 = iron (11) tetraoxosulphate (VI) heptahydrate CuS04. 5 H z 0 = copper (11) tetraoxosulphate (VI) pentahydrate In the above nomenclature "-hydratep' refers to a molecule of water ~k~stallization while the Greek prefix shows the number of molecules of such water of crystallization associated with the saIt. Another acceptable method of expressing the water of crystallization is as follows: Na2C03.10HzO = sodium trioxocarbonate (1V)-10-water MgS04 7H20 = magnesium tetraoxosulphate (V1)-7-water FeS04.7Hz0 = iron (11) tetraoxosulphate (V1[)-7-water CuS04.5H20 = copper (11) tetraoxosulphate I(VI)-5-water -- - - -. In this method the numbers 10, 7, 7, and 5 indicate the number of water of crystallization respectively. A third alternative makes use of a combination of the Greek p r e h and the Latin-derived word "aquo", such that: . a. Na,CO3. 10H20= sodium decaaquotrioxocarbonate (IV) MgS04. 7H20 = magnesium heptaaquotetraoxosulphate (VI) FeS0,. 7H20 = iron (11) heptaaquotetraoxosulphate (VI) CuS04.5H90 = cooDer (11) ~entaaauotetraoxosulphate(VI) DOUBLE SALTS: GUIDELINES FO AND NOMENCLP (i) in writing the formulae of double sa placed first and then followed by the anions. 1 in order of inc;easing valence (except hydro1 ~tionsare arranged Exumples: In KMgF3, the cations are K+ and M ~ ~Ki + , the formular in increasing order of valenc valence also explains the order in which the cations appear in: NH4MgP04.6H20, cations: NH: and ~ g ~ + (NH4)2Fe (SO,&.6H20, cations: NH; and Fe2+ (ii) When two or more cations have the same valence, they are arranged in order of decreasing atomic number, with the polyatomic ions. (e.g. ammonium, NHZ) at the end of the appropriate valence group. In KNaC03, the cations K + and Na+ are in the same valence group. These are, therefore, arranged i,n order of decreasing atomic number. The atomic number of potassium is 19 while that of sodium is 11. In TINa(NO&, the cations TIi and Nat--arein the same valence group and so are arranged in order of decreasing atomic number: TI (atomic number = 81), Na (atomic number = 11). (iii) When hydrogen is present as a cation (acidic hydrogen) the symbol is placed last among the cations. NaNH4HP0,.4H20. Here NH; is polyatomic and so comes after Na+ according to guideline (ii). H+ comes last among the cations on the basis of guideline (iii). (iv) Anions present in double salts are cited in the following group order: 1. 1-I2. 0*- and O H - (in that order) 3. o n e element inorganic anions other than H- and 02-.(The order of appearance is: 0, Si, C, Sb, As, P, N, T e , S e i S , At, I, Br, CI, F) 4. Inorganic anions containing two or more elements, other than OH-. (In citing this group of anions, anions with the smallest number of atoms, are cited first. For two anions with the same number of atoms, they are cited in order of decreasing i t o mic number of the central atoms). Exumples: (v) In naming double salts, the component cations and anions are named as illustrated for cations and anions in simple saks. However, the cations present in the formula are named in alphabetical order. Illustrative examples: KNaCO,: potassium sodium trioxocarbonate (IV) KMgF3: magnesium potassium fluoride sodium thallium (1) trioxonitrate (V) TINa(N03),: NH4MgP04.6 H 2 0 : ammonium magnesium tetruoxophuspharc (V) hexahydrate amnloniurn iron (11) tetraoxusulphate (VI) (NH,)*Fe(SO,),: NaNH,HPO, . 4H20: sodium ammonium hydrogen tetraoxophosphate (V) tetrahydratc NH4AI(S04)2: aluminium amn~uniumt ~ t r a ~ x o s u l p h i i (t eV l ) (hexa) sodium chloride tluoride ( b ~ s ) Na6CIF(S04),: tetraoxosulphate Ca5F(P04)3: (penta) calciumfluoride (tris) tetraoxophosphate KAI(SO,), . 121-I2D: aluminium potassium bis [tetraoxosulphatc (VI)] dodecahydrate THE HALIDES OF CAI Although these halides of carbon be organic chemistry and are better discuss1 thcre is need to underscore their IUPA can be found in inorganic texts as well rccommcndation, these group of com carbontetrahalides are to be regarded a> of halogen atoms per molecule being sp CF4 CClj CBr4 CI, CIiCI CHBr3 = = = = ,= = C:H2C12 = CHI3 Cb = tetruHuoromethane tetrachloromethane tetrabrom~methitn~ tetraiodomethane trichlorornethane tribron~omethant: dichioromcthane triiodomethane Free radicals are odd electron molecules or atoms. Most ot' then1 are electrically neutral (a few radical ions arc: known). All possess addit~onproperties and are extremely reactive. Example: It is normal to represent the symbol o r formula of it radical with a dot to signify the add electron. Names of radicals have two components: the name of the element or group plus the word "radical." Examples: F' CI' Br' I' CH; fluorine radical chlorine radical, bromint: rcldical iodine radical methyl radical FORMULAE AND NAMES 01:COMPO We can now summarize some of the highli writing formulae and naming of inorganic c In writing a chemical formula the ele, (cation) is written first before the clectron KCI, nor CIK; NH,NO,, not N 0 3 N H 4 ) . If the compound contains more than o r tuent, these are arranged in order of increa When a binary compound is formed I constituent which appears earlier in the sc first. Sequence: B, Si, CjSb, As, P, N, H, TI F. E.g., NH3, not H,N. The number of identical atoms o r atomic groups in a formula is indicated by means of Arabic numerals, placed below and t o the right of the symbol or symbols in piirenthesis ( ) o r brackets [ ] to which they refer. E.g., CaCI2, not CaC12; (NM,)2S0,, not 2(NH4)SO,. However, .water of cryskdlization and similar loosely bound rnolccuks are designated by means of Arabic nunwrals bufore their formulae. E.g., Na2S0,. 10H20. ? h c charge on thc formula of an ion reprcsuuts tllc arilhnlclic sum of the oxidation numbers of aH-the con~titucntatoms. In NH:, sum of oxidation numbers = -3 for N plus +4 for 4(Hj, giving a net + 1 charge. In SO;-, sum of oxidation numbers = + 6 for S plus -8 for 4(0) = -2. The systematic names of compounds ure formed by indicating the conslit uents and their proportions. The stoichimetric proportion of the constituents may be expressed in the name of a compound by means of Greek nurnerical prefixes (mono, di ... ) preceding without hyphen the names of the elements t o which they refer. E.g. N,O (dinit rogen oxide), NO2 (nitrogen dioxide). However, the Stock's system has gained the upper hand. In this system, the proportions of constituents are indicated indirectly ... als representing the oxidatidn number or stoichiometric valence of the element. This is placed in parenthesis immediately following the name of the atom to which it refers. Exumples: N 2 0 nitrogen (I) oxide NOz nitrogen (IV)oxide FeClz iron (11) chloride The name of the electropositive constituent (or that treated as such) is not modified. Examples CaO (calcium oxide), AgCl (silver chloride), I n a compound in which the electronegative constituent is monoatomic, the name of the compound ends in "-ide). Examples: (NH,),S (ammonium sulphide). However, when the electronegative constituent is polyatomic, the name (with a few exceptions) ends in "-atew. E.g. NH4N03 ammonium~trioxonitrate(V). The terms sulphate, nitrate, phosphate, etc., were originally assigned to anions of particular 0x0 acids. These terms are now used more generally for any negative group containing sulphur, nitrogen, phosphorus, etc., respectively, as the central atom, irrespective of its oxidation state and the number and nature of the ligands. sodium tetraoxcwulphare (VI) sodium trioxosulphate (IV) sodium trioxothicxrulphate (11) sodium trioxofluorosulphate (VI) sodium tetraoxophosphute (V) sodium tetrathiophosphate (V) sodium hexachlorophosphate (V) potassium dioxodifluorophosphale (V) potassium oxodichloroimidophosphate Names such as sodium sulphate, sodium thiosulphate, etc., can now be regarded as abbreviations in the above system of nomenclature. . FORMULAE AND IUPAC NAMES OF SOME COMMON COMPOUNDS AND IONS Formula Name AgCl AgN03 ALC3 silver chloride silver trioxonitrate (V) aluminium carbide aluminium (111) oxide arsenic (111) oxide barium (11) oxide barium (11) peroxide barium tetraoxosulphate (VI) bismuth (111) chloride oxide bromide ion calcium dicarbide calcium dichloride calcium trioxocarbonate (1V) calcium hydrogen trioxwarbonatc (Icalcium oxide calcium hydroxide calcium tetraoxosulphate (VI) tetrabromomethane tetrachioromethane tetrafluoromethane trichloromethane tribromomethane dichloromethane tetraiodomethane carbon (11) oxide carbon (IV) oxide trioxocarbonate (IV) ion chromium (11) oxide chromium (111) oxide chrdmium (VI) oxide chromium (111) sulphide A1203 As203 BaO Ba02 BaSO, BiOCl BrCaC2 CaCll CaC03 Ca (H C03)2 CaO #"(OW2 CaSO, CBr4 CCI, CF4 CHC13 CHBr-, CH2C12 Cl4 CO COz co: CrO (3203 CrOJ (32% CrSO,, -' copper (TI) chloride dicopper (11) frioxocarbonate (IV) dihydroxide copper (11) oxide copper (1) oxide tetraarnine copper (11) dichloride copper (11) hydroxide copper (11) chloride trihydroxide copper (11) tetraoxosulphate (VI) capper (11) tetraoxosulphate (VI) pentahydrate iron (If) chloride iron (111) chloride iron (11) oxide iron (111) oxide triiron tetraoxide iron (11) hydroxide iron (111) hydroxide iron (IS) s u l ~ iron (11) tetr e (v1) e (VI) heptahydrate iron (11) tetr iron (111) tetraoxosulpnate (V1) hydrogen bromide acid hydrogen chloride acid mercury (I) chloride mercury (11) chloride hydrogen fluoride acid hydrogen iodide acid trioxonitrate (1V) acid trioxonitrate (V) acid tetraoxophosphate (V) acid tetraoxosulphate (IV) acid tetraoxosulphate (VI) acid iodine (I) chloride iodine (V) oxide aluminium potassium bis [tetraoxosulphate,(VI)] dodecahydrate potassium bromide potassium heptaoxodichromate (VI) potassium monoxchlorate (I) potassium trioxochlora te (V) potassium hexac:yanoferrate (11) potassium hexac:yanoferrate (111) potassium iodidcrn potassium tetrac~xomanganate(VII) potassium tetracyanonicollate (0) potassium oxide potassium tetrac~xosulphate(VI) magnesium chloride magnesium oxidle magnesium h y droxide ~ magnesium chlaride hydroxide magnesium tetrlioxosulphate (VI) magnesium tetriioxosulphate (VI) heptahydrate manganese (I I) chloride manganese (11) oxide manganese (IV) oxide manganese (111) oxide trimanganese tetraoxide manganese (11) tetraoxosulphate (Vl) sodium hexafluoroalumnate (111) sodium chloride sodium monoxchlorate (I) sodium trioxochlorate (V) sodium trioxocarbonate (IV) sodium hydride sodium hydrogen trioxocarbonate (IV) sodium dihydrogen tetraoxophosphate (V) sodium hydrogen trioxosulphate (IV) sodium hydrogen tetraoxosulphate (VI) dioxonitrate (111) ion srioxonitrate (V) ion sodium hydroxide sodium trioxosuiphate (IV) sodium tetraoxosulphate (IV) ammonium ion ammonia solution amrnooium dioxonitrate (111) ammonium trioxonitrate (V) aluminium ammonium tetraoxosulphate (VI) w NaCl NaClO NLICIO~ Ni12C03 NaH NaliC03 NaH,IJ04 NallSO, NaHSO, NO; N 0, NaOI-I Na2S03 Na2S04 NH: NHIOH N H4NO2 NH4N03 NI 14AI(S04)2 (NH4)2Fe(S04)2 N2O NO NO2 N204 IY2@ amnfonium iron (II) tetraoxosulphate (Vl) nitrogen (I) oxide nitrogen (11) oxide nitrogen (IV) oxide dinitrogen tetraoxide nitrogen (V) oxide nitroeen (VI\ oxide NO, NiO Ni02 Ni(OH)* nicl nicl nickel (11) hydrOXld& PbCl, PbCI3 le le PbCIS PO:poi- le terraoxopnospnarc ( vl) ion tetraoxophosphate (V) ion tetraphosphorus dccaoxidt lead (11)I bxide lead (IV') oxide trilead trmaoxide lead (11)I sulphide- lead (11) tnoxosulphate (N) lead (11) tetraoxosulphate (VI) lead (11) trioxonitrate (V) phosphorus (UI) chloride phosphorus (V) chloride antimony (111) oxide silican (IV)oxide sulph~ u r(IV) oxide sulphbur (VI) oxide trioxosulpnare (I v ) Ion tetraoxosulphate (V1) ion zinc 1oxide zinc chloride zinc tetraoxosulphate (V 1) P4O10 PbO PbOz bO4 PbS PbS03 PbS04 Pb(NW2 PC13 PCIS Sb203 Si02 SO2 SO3 so: so;ZnO ZnCI, ZnSOJ a rn A I,.,\ !- 1 bxochlorate (I) ion trioxochlorate (V) ion tetraoxochlorate (VII) ion trioxocarbonate (IV)ion heptaoxod I L I ~ I U I I I ~ C C\; v I) ion hydrogen Itrioxocarbonate (IV) ion tetraoxom;angiinate (Vl) ion tetraoxom;anganate, (VlI) ion dioxonitraite (111) i on trioxonitra te (V) ic>n trioxosulpilate (IV: I ion tetraoxmu lphate (1f1) ion thiosulpha~ te ion or tfioxosuIp~ ~ursulphi 3te (IV) ion tetrathiona~ t eor hexaoxodhrulphurd!isulphare (V) ion persulphatie or hexaoxope roxodisu lphate (VI) ion Basic Salts ,...-. BiOCl Mg(0H)CI PbzCOdOH)2 bismuth (I,,, ide oxide magnesium chloridle hvdroxide dilcad (11) trioxocarbok (IV) diL-+"---:-'- W o u b l e Salts Fe(NH&(SO,) ,.6 H 2 0 diammonium iron (11) bis KAI (SO&. 12H20 [tetraoxosuIphate (VI)]-bexahyc aluminium potassium bis [tetraoxosulphate (VI)]-dodecal Complex Ioru diamminesilver (I) ion tetrahydridoalurninate (111) ion tetrahydroxodiaquaalurninate (111) ion tetrahydridoborate (111) ion diammine copper (I) ion tetraamminecopper (11) ion hexacyanoferrate (11) ion hexacytlnoferrate (UI)ion oxonium ion or hydronium ion or hydroxonium ion ammonium ion tetraammine zinc (11) ion 9. Give the chemical formulae of the following compounds: (i) sulphur (11) chloride (ii) bromine (111) fluoride (iii) manganese (IV) oxide (iv) mercury (11) chloride ( v ) niolybdc~~um (VI) oxidc (vi) dinitrogen tetroxide (vii) diphosphorus pel-- ' ' (viii) dichloromethane 10. The following names have been submitted by students for the compounds and ions indicated. Each is wrong in at Icilst orie respect. Indicate what is wrong in each case: (i) MnFJ manganic fluoride (ii) F e S 0 4 .'lh& iron (111) tetraoxosulphate (VI) pentahydrate (iii) NO, trioxonitrate (111) ion (iv) NaCIQ3 sodium oxochlorate (1) (v) SO$tsioxosulphate (IV) ion THE PERIODIC TABLE OF ELEMENTS a 1I.i ! 4 6.841 9.U1218 I1 19, Na u.esw7 JV.lHll Rb 85.4671 55 8 He 10.111 Mg tr.31~~ 4I.lMJ 38 U.VS59 Sr 87.152 1.9059 56 7 22 5B 23 47.W 50.9414 411 V 6B 78 24 .25 Cr 5I.M OB 26 27 2E 511.70 Mn Fe Co Y.Y.7WI 55.847 5A.9332 I Se Br 7H.'& 79.WM SO 51 52 53 5. IIJ.l$2 Ilb.bY 121.75 127.W lb.W+5 Irl.30 81 82 83 X4 85 At Hn Gu , Ge 69.72 9S.M 98.YUbZ 101.07 l%2.9WS 106.4 107.4WI 77 78 79 132.9(%4 IJ7..U 138.W55 178.49 IOO.llJ7Y 1113.m 186.287 1Bt.L 192.22 39.619 As 7,n b5.33 73 Yf J.~..Jz) 74.V116 Cu 9Z.W Ir At- 72.59 2 8 . 0 ~ 30.9737~ JZJM 63.544 72 0s IH Cl 32 91.22 Re D.17V 31 Rh W 34 17 w.carsr Ru l'a 13 S 10.WKIY 30 Tc Hf f !h 2B Mo *La IS.% 29 Nb Ba I.I.Ulf67 1B Zr Cs IZ.UII 10 Au 112.40 4; TI Ph Ili R, HJ. 86 APPENDIX 2: OXI9ATION STATES OF ELEMKNTS 1N THE PERIODIC TABLE. WHERE A N ELEMENT CAN HAVE MORE THAN ONE 0XIL)ATION STATES, THE MOST COVMON O N K 1s GIVEN IN BOLD TYPE. Groups APPENDIX 3: TADLE OF ELEMENTS, SYMBOLS, A'TOMIC NUMBER A N D RELATIVE ATOMIC MASSES. THE ArTOMlC MASSES AWE BASED ON CAHBO?Y-12. Symbol Actinium Alun~inum Americium Antimony Argon Arsenic Astatine Hariunr Lferkellum Beryllium Bisniuth Boron Bromine Cadmium Calcium Cali&rnium Carbon Cerium Cesium Chlorine Chromium Cobalt Copper Curium Dysprosium Einsteinium Erbium Europium Fermium Fluorine Francium Gadolinium Gallium Germanium Gold Hatnium Ac Al Am Sb Ar As At Ba Bk Be Bi U Br a Ca Cf C Ce Cs CI cr eo Cu Cm DY Es E; Ell bm F Fr Gd Gn Ge Au HI No. Atomic Muss 12271 P433' 121.75 137.34 208.980 J 10.81 79.w 112.40 40.08 W I 12.01 1 140.12 132.ws4 35,453 51.996 58.9332 63.546 r2471 162.50 12541 167.26 151.96 12571 18.99840 P I 157.25 69.72 72.59 196.966 5 178.49 1 lelium Holmium 1-1ydrogen Indium Iodine Iridium Iron Krypton Lanthanum Lawrencium I-cad Lithium 1.11terium Mitgncsium hlangancse Mendelevium Mercury Molybdenum Neodymium Neon Neptunium Nickel Niobium N~trogen Nobelium Osmiuni Oxygen I'~ilIidi~i~~ Phosphorus Platinum Plutonium Poionium Potassium Praseodymium Promethium Protactinium Kadium Radon Rhenium Rhodium Rubidium IWhenium Samarium Scandium Selenium Silicon Silver Sodium Strontium Sulfur Tantalum Technetium Tellurium Terbium Thallium Tl~oriun~ Thulium Tin Titanium Tungsten Uranium Vanadium Xenon Ytterbium Yitriunl Zinc Zirconium e 'A value given in brackets denotes the mass number of the isotope. 11. Give (i) (ii) (iii) (iv) systematic names for the following KCaPO, NaHC03 NO CrC03 (v) Ag2F APPENDIX 4: ANSWERS TO NUMERICAL QUESTIONS 2. :;K+ 3. (i) t 6 (ii) 4-6 (iii) +2 4. (a) - 1 , + I , +3, and +7 respectively. (b) +6, +4, +7, +2:; and 7 respcctivcly. (c) +3, +6$, +6, -t6, and $3 rcspectively. 5. (a) +3, -2 (b) +2, t 3 , -2 (c) $ 5 , - 1 (d) +3, -2 (e) +6, -2 (f) -? 6. (a) +4 (e) + 3 (f) -1 (b) +2 (d + 2 (c) +7 (d) I-6 (h) + 6 7. (i) chromium changed oxidation number from +6 to + 3 (ii) oxygen changed oxidation number from -2 to O 8. Oxid. No. of Reactants Oxid. No. of Products +7 Mn 0 -2 C1 -1 +2 -2 O H +1 -t 1 (i) SOCI, (ii) BF,3 (iv) I-IgCI, (iii) h1110, (v) hlo0.3 (vi) N,O, (vii!) CH2CI2 (vii) P 2 0 5 10. The correct names are: (i) manganese (IV) fluoride , (VI) hcptahydra~e (ii) iron (11) te~raoxosulpha~e (iii) trioxonitrate (V) ion (IV) sodium trioxochlornte (V) ( v ) t ~ . i ~ ~ o s u l p h i(1V) i t e ion 11. (i) cdcium potassium tetraoxophosphate ( V , (ii) sodium hydrogen trioxocarhonate (1V) ( i i i ) nitrogcn (11) oxide (iv) chromium (!I) triost)carbonrttc (IV) (v) disilver rno~wfluoridt: 9. 1 APPENDlX 5: GLOSSARY i d : a substance which on being diswlved in water produces a solution in which the hydrogen ion concentration is greater than 1 W 7 ~Exam. ples: H2S04, H N 0 3 , HCI, H2C03. allotropy: the property which some elements possess of existing in different forms with different properties. The chief differences are' usually found in the physical properties, though there are sometimes differences in the chemical propeities as well. The different forms of the element are called allotropes, or allotrcrpic modifications. Example: O2 and 03. am&~tericoxide: an oxide which can function both as a basic oxide and as an acidic oxide, depending on reaction conditions. Examples: ZnO, A1203. anion: an ion that is negatively charged. Examples: C1-, SO:-, NO;. atomic number: the number of protons in the atomic nucleus, and hence the number of unit positive charges on the nucleus. It also represents the nuniber of extranuclear electrons in an atom. base: a substance which on being dissolved in water produces solution in which hydroxide ion concentration is gredter than 10-'M. fianlples: NaOH, KOH, NH3. cation: an ion that is positively charged. Eramples: Li+,Ca2+, AP+, electronegativity: a measwe of the tendency of an atom to attract shared electrons. electropositive refen to elements whose atoms tend to lose elements: elections easily. Examples: Li, Na, K,Ca, Mg. ion : a charged species; an entity chrryinp either positive or negative charge. Fsanrples: CI- , SO:-, NHZ, Ca2+ different kinds of atoms of the same element. They have the same atomic number (and consequently they have t h e same arrangemnt of extranuclear electrons and hence the same chemical properties). They differ solely in having different mass numbers on account of. having different numbers of neutrons on the nucleus. Example: the three isotopes of oxygen are: '20, I@, '@ isotopes: ligand: neutralization: a species bonded to the central atom in a complex ion. Examples: H 2 0 in [ A I ( H ~ o ) ~ J ~ + , OH in [Zn(OH),I2- a term used to describe the reaction between an acid and a base t o give a neutral (sah) solution. nonpolar bond: a chemicat bond in which there are no positive and negative ends; mainly found in homonuclear diatomic molecules such as CI,, 0 2 ,H2. periodic table: an arrangement of the elements into rows and columns such that elements with similar properties occur in the same column. I I I I I