• Study Resource
  • Explore Categories
    • Arts & Humanities
    • Business
    • Engineering & Technology
    • Foreign Language
    • History
    • Math
    • Science
    • Social Science

    Top subcategories

    • Advanced Math
    • Algebra
    • Basic Math
    • Calculus
    • Geometry
    • Linear Algebra
    • Pre-Algebra
    • Pre-Calculus
    • Statistics And Probability
    • Trigonometry
    • other →

    Top subcategories

    • Astronomy
    • Astrophysics
    • Biology
    • Chemistry
    • Earth Science
    • Environmental Science
    • Health Science
    • Physics
    • other →

    Top subcategories

    • Anthropology
    • Law
    • Political Science
    • Psychology
    • Sociology
    • other →

    Top subcategories

    • Accounting
    • Economics
    • Finance
    • Management
    • other →

    Top subcategories

    • Aerospace Engineering
    • Bioengineering
    • Chemical Engineering
    • Civil Engineering
    • Computer Science
    • Electrical Engineering
    • Industrial Engineering
    • Mechanical Engineering
    • Web Design
    • other →

    Top subcategories

    • Architecture
    • Communications
    • English
    • Gender Studies
    • Music
    • Performing Arts
    • Philosophy
    • Religious Studies
    • Writing
    • other →

    Top subcategories

    • Ancient History
    • European History
    • US History
    • World History
    • other →

    Top subcategories

    • Croatian
    • Czech
    • Finnish
    • Greek
    • Hindi
    • Japanese
    • Korean
    • Persian
    • Swedish
    • Turkish
    • other →
 
Profile Documents Logout
Upload
Unit 13: Organic Chemistry
Unit 13: Organic Chemistry

... • An ether is an organic compound containing an oxygen atom bonded to two carbon atoms • Ethers are named by listing the two groups attached before the word ether • If the two groups attached are the same the ether is named by putting di- in front ...
Chapter 21 Worksheet
Chapter 21 Worksheet

... 1. Find the longest continuous carbon chain (parent chain). a. If there is a functional group (double or triple bond, alcohol etc) it must be on or part of the parent chain. b. If there is a ring in the compound either the ring itself or the non-ringed chain will be the parent chain but never both c ...
Organic Reactions Summary Sheet
Organic Reactions Summary Sheet

... chloroform ...
Lecture Resource ()
Lecture Resource ()

... • Some amines are heterocyclic compounds (or heterocycles) • Most drugs, vitamins, and many other natural products are heterocycles • A natural product is a compound synthesized by a plant or an animal ...
C14_-_Organic_Chemistry
C14_-_Organic_Chemistry

... 14.2 Introduction to organic compounds ...
Aldehydes and Ketones
Aldehydes and Ketones

... How can we tell if we’ll be getting carbonyl addition or conjugate addition? Fortunately, it is quite easy. Non-carbon nucleophiles (we frequently call these “soft” nucleophiles) like nitrogen (amines) and oxygen (alcohols) will always add in a conjugate fashion, particularly if the reaction is carr ...
Organic Chemistry - Unit 2
Organic Chemistry - Unit 2

... (Substituted benzene) In all of these compounds, the halogen is considered to be the functional group. Very few halocarbons exist in nature but they are easily produced in substitution reactions. Alcohols Alcohol – an organic compound containing at least one hydroxyl group. ( – OH ) group. The hydro ...
Chapter 5
Chapter 5

... Contents of Chapter 4 ...
I PUC Chemistry Mock Paper
I PUC Chemistry Mock Paper

... 14. How is plaster of paris prepared from gypsum? Give equation 15. Write any two differences between diamond and graphite. 16. Explain Wurtz reaction with an example. 17. How do you convert benzene to hexachlorobenzene ? Give equation 18. Mention any two gases which are responsible for greenhouse e ...
Group 2 - UC Davis Canvas
Group 2 - UC Davis Canvas

... 11. The bond energy of the noble gas fluorine is too small to offset the energy required to break the F—F bond. 13. Iodide ion is slowly oxidized to iodine, which is yellow-brown in aqueous solution, by oxygen in the air: 4 I − ( aq ) + O 2 ( g ) + 4 H + ( aq )  → 2 I 2 ( aq ) + 2 H 2 O(l) . 15. D ...
Substitution Rxns
Substitution Rxns

... Tertiarary (3) alcohols cannot be oxidized by acidified K2Cr2O7 as they have no hydrogen atoms attached directly to the carbon atom containing the –OH group.  It is not true to say that tertiary alcohols can never be oxidized, as they burn readily. However, when this happens the carbon chain is de ...
Abbreviated Chapter 17 Powerpoint
Abbreviated Chapter 17 Powerpoint

... • The nitro group is a strongly deactivating group when considering its resonance forms. The nitrogen always has a formal positive charge. • Ortho or para addition will create an especially unstable ...
Organic Chemistry - GZ @ Science Class Online
Organic Chemistry - GZ @ Science Class Online

... oxidant such as dichromate or permanganate is used. Polymerisation reactions join monomers together to form a polymer. Addition polymerisation breaks double bonds of alkenes and joins monomers Condensation polymerisation removes a molecule of water (H from one monomer and OH from another) and joins ...
Alkenes from Alcohols
Alkenes from Alcohols

... Alkenes from Alcohols 2-Methyl-1-butene and 2-Methyl-2-butene INTRODUCTION The dilute sulfuric acid catalyzed dehydration of 2-methyl-2-butanol (t-amyl alcohol) proceeds readily to give a mixture of alkenes. The mechanism of this reaction involves the intermediate formation of the relatively stable ...
Nucleophilicity and Basicity Factors in Organic Reactions
Nucleophilicity and Basicity Factors in Organic Reactions

... occurs when a vicinal (adjacent) atom carries a non-bonding electron pair. Two common examples of this exception, called the alpha effect, are hydroxide ion (pKa 15.7) compared with hydroperoxide ion (pKa 11.6), and ammonia (pKa 9.3) compared with hydrazine (pKa 8.0). In each of these pairs the weak ...
Carbon Compounds
Carbon Compounds

... What do you mean by allotropes? Name three allotropes of carbon. Write 2 points of difference in the structures and properties of diamond and graphite. What is Buckminster fullerene? How many atoms does its molecule contain? Why is diamond used for making cutting tools? What do you mean by catenatio ...
WEEK 7
WEEK 7

... and the molecular formula is C3H8. Notice that carbon always has four bonds attached to it. The molecular formula is determined by counting the number of carbons and the number of hydrogens. There is a fixed ratio between carbon and hydrogen in alkanes that can be expressed by a TYPE FORMULA: CnH2 ( ...
Organic Families: Summary Chart
Organic Families: Summary Chart

... The more C atoms present, the harder it is to break the bonds. The more C atoms, the higher the boiling point. Alkenes and alkynes are more reactive than alkanes due to their double/triple bonds (unsaturated). Presence of OH group makes alcohol more polar than hydrocarbons. Therefore, boiling point ...
Chem 3.5 Answers #6
Chem 3.5 Answers #6

... For primary and secondary amines, the presence of the N-H bond enables the amine molecules to hydrogen bond to water molecules. This allows them to dissolve in water. With higher Mr this solubility decreases. Although both primary amines and alcohols can form hydrogen bonds to each other, the hydrog ...
Nucleophilic Substitution Reactions
Nucleophilic Substitution Reactions

... ■ Nucleophiles are reactants that are electron rich, as they have a lone pair of electrons and may also carry a negative charge. These species are therefore attracted to the electron-deficient carbon atom in the halogenoalkane. ...
CH 3
CH 3

... • Boiling Points: Compounds with hydrogen bonding have higher than expected boiling points: at SATP, C2H6 = gas but CH3OH = liquid. • Solubilities: Compounds with hydrogen bonds are usually soluble in water (a polar molecule): C6H14 = insoluble in water but C5H11OH = soluble in water. • Solubility d ...
CH 3
CH 3

... • Boiling Points: Compounds with hydrogen bonding have higher than expected boiling points: at SATP, C2H6 = gas but CH3OH = liquid. • Solubilities: Compounds with hydrogen bonds are usually soluble in water (a polar molecule): C6H14 = insoluble in water but C5H11OH = soluble in water. • Solubility d ...
Chapter 3
Chapter 3

... Common names are still used for some alkenes and alkynes, particularly those with low molecular weight. ...
Chapter23
Chapter23

... Up until this point, we have considered organic molecules of low molar mass, but some of the most important organic molecules are giant molecules called polymers. You see polymers everyday. All plastics are polymers and so is the miracle molecule DNA, which is responsible for nearly all the life for ...
Unit 2 Summary Booklet
Unit 2 Summary Booklet

... Saturated hydrocarbons contain only C-C single bonds. o The alkanes are saturated hydrocarbons. o The cycloalkanes are saturated hydrocarbons. Unsaturated hydrocarbons contain C=C double bonds. o The alkenes are unsaturated hydrocarbons. The bromine solution test can be used to distinguish between s ...
< 1 ... 135 136 137 138 139 140 141 142 143 ... 171 >

Haloalkane



The haloalkanes (also known, as halogenoalkanes or alkyl halides) are a group of chemical compounds derived from alkanes containing one or more halogens. They are a subset of the general class of halocarbons, although the distinction is not often made. Haloalkanes are widely used commercially and, consequently, are known under many chemical and commercial names. They are used as flame retardants, fire extinguishants, refrigerants, propellants, solvents, and pharmaceuticals. Subsequent to the widespread use in commerce, many halocarbons have also been shown to be serious pollutants and toxins. For example, the chlorofluorocarbons have been shown to lead to ozone depletion. Methyl bromide is a controversial fumigant. Only haloalkanes which contain chlorine, bromine, and iodine are a threat to the ozone layer, but fluorinated volatile haloalkanes in theory may have activity as greenhouse gases. Methyl iodide, a naturally occurring substance, however, does not have ozone-depleting properties and the United States Environmental Protection Agency has designated the compound a non-ozone layer depleter. For more information, see Halomethane. Haloalkane or alkyl halides are the compounds which have the general formula ″RX″ where R is an alkyl or substituted alkyl group and X is a halogen (F, Cl, Br, I).Haloalkanes have been known for centuries. Chloroethane was produced synthetically in the 15th century. The systematic synthesis of such compounds developed in the 19th century in step with the development of organic chemistry and the understanding of the structure of alkanes. Methods were developed for the selective formation of C-halogen bonds. Especially versatile methods included the addition of halogens to alkenes, hydrohalogenation of alkenes, and the conversion of alcohols to alkyl halides. These methods are so reliable and so easily implemented that haloalkanes became cheaply available for use in industrial chemistry because the halide could be further replaced by other functional groups.While most haloalkanes are human-produced, non-artificial-source haloalkanes do occur on Earth, mostly through enzyme-mediated synthesis by bacteria, fungi, and especially sea macroalgae (seaweeds). More than 1600 halogenated organics have been identified, with bromoalkanes being the most common haloalkanes. Brominated organics in biology range from biologically produced methyl bromide to non-alkane aromatics and unsaturates (indoles, terpenes, acetogenins, and phenols). Halogenated alkanes in land plants are more rare, but do occur, as for example the fluoroacetate produced as a toxin by at least 40 species of known plants. Specific dehalogenase enzymes in bacteria which remove halogens from haloalkanes, are also known.
  • studyres.com © 2026
  • DMCA
  • Privacy
  • Terms
  • Report