110A Exam 1 Review Sheet-Fall Semester 2016 Review Session
... 6. Be able to write valid Lewis structures and assign formal charges in small molecules. 7. Be able to apply VSEPR theory to a molecule and explain a case where theory is accurate and a case where the theory is not. 8. Be able to write down the atomic orbitals for any first-row atom, using C as an e ...
... 6. Be able to write valid Lewis structures and assign formal charges in small molecules. 7. Be able to apply VSEPR theory to a molecule and explain a case where theory is accurate and a case where the theory is not. 8. Be able to write down the atomic orbitals for any first-row atom, using C as an e ...
this PDF file
... reduced reagent precipitated. The progresses of the reactions were monitored by TLC and UV/Visible spectrophotometer (at 352 nm). Analysis of the reaction mixture for the corresponding carbonyl compound was accomplished by the procedure reported in earlier papers. [9, 10]. The above procedure may be ...
... reduced reagent precipitated. The progresses of the reactions were monitored by TLC and UV/Visible spectrophotometer (at 352 nm). Analysis of the reaction mixture for the corresponding carbonyl compound was accomplished by the procedure reported in earlier papers. [9, 10]. The above procedure may be ...
McMurray-Fay Chapter 22 Presentation Slides
... 2 CH3CH2CH2CH3(g) + 13 O2(g) → 8 CO2(g) + 10 H2O(g) CH3CH=CHCH3(g) + 6 O2(g) → 4 CO2(g) + 4 H2O(g) 2 CH3CCCH3(g) + 11 O2(g) → 8 CO2(g) + 6 H2O(g) ...
... 2 CH3CH2CH2CH3(g) + 13 O2(g) → 8 CO2(g) + 10 H2O(g) CH3CH=CHCH3(g) + 6 O2(g) → 4 CO2(g) + 4 H2O(g) 2 CH3CCCH3(g) + 11 O2(g) → 8 CO2(g) + 6 H2O(g) ...
11.2 Types of Chemical Reactions
... These equations describe two examples of single-replacement reactions. A single-replacement reaction is a chemical change in which one element replaces a second element in a compound. You can identify a singlereplacement reaction by noting that both the reactants and the products consist of an eleme ...
... These equations describe two examples of single-replacement reactions. A single-replacement reaction is a chemical change in which one element replaces a second element in a compound. You can identify a singlereplacement reaction by noting that both the reactants and the products consist of an eleme ...
CH 20: Carboxylic Acids and Nitriles
... • Oxidation of a substituted alkylbenzene with KMnO4 or Na2Cr2O7 gives a substituted benzoic acid (see Section 16.9) • 1° and 2° alkyl groups can be oxidized, but tertiary groups are not ...
... • Oxidation of a substituted alkylbenzene with KMnO4 or Na2Cr2O7 gives a substituted benzoic acid (see Section 16.9) • 1° and 2° alkyl groups can be oxidized, but tertiary groups are not ...
Alcohols, Phenols, and Thiols
... • is the IUPAC name for benzene with a hydroxyl group. • is used in antiseptics and disinfectants. ...
... • is the IUPAC name for benzene with a hydroxyl group. • is used in antiseptics and disinfectants. ...
CHE2060 Syllabus - Joan`s courses
... Moodle links to my course web site: richmond-hall.weebly.com/che2060.html This course is designed to introduce students to the study of organic chemistry, and serves as a comprehensive introduction to the subject. Material includes a general overview of the basic organic compounds, from alkanes to h ...
... Moodle links to my course web site: richmond-hall.weebly.com/che2060.html This course is designed to introduce students to the study of organic chemistry, and serves as a comprehensive introduction to the subject. Material includes a general overview of the basic organic compounds, from alkanes to h ...
CH - UTH e
... Grignard, Victor , 1871–1935, French chemist. He shared the 1912 Nobel Prize in Chemistry for his work in organic synthesis based on his discovery (1900) of the Grignard Reagent. He taught at the Univ. of Nancy (1909 Grignard Reagent. He taught at the Univ. of Nancy (1909–19) 19) and at the Univ. ...
... Grignard, Victor , 1871–1935, French chemist. He shared the 1912 Nobel Prize in Chemistry for his work in organic synthesis based on his discovery (1900) of the Grignard Reagent. He taught at the Univ. of Nancy (1909 Grignard Reagent. He taught at the Univ. of Nancy (1909–19) 19) and at the Univ. ...
structure and substitution. Thus, the culties associated with
... will be as useful in the detection of chain branching as is the case for the alkenes. Because the alkyne range of chemical shifts overlaps those of the alkanols and aliphatic ethers, ...
... will be as useful in the detection of chain branching as is the case for the alkenes. Because the alkyne range of chemical shifts overlaps those of the alkanols and aliphatic ethers, ...
OR Practice Problem - HCC Southeast Commons
... Alcohols are named according to the IUPAC system 1. Select the longest carbon chain containing the OH group, and derive the parent name by replacing the -e ending of the corresponding alkane with -ol 2. Number the chain from the end nearer the OH group 3. Number substituents according to position on ...
... Alcohols are named according to the IUPAC system 1. Select the longest carbon chain containing the OH group, and derive the parent name by replacing the -e ending of the corresponding alkane with -ol 2. Number the chain from the end nearer the OH group 3. Number substituents according to position on ...
MECH 558 Combustion Class Notes
... Before learning how hydrocarbons react with oxygen in flames, we must first go over some nomenclature for the different classes of hydrocarbons. 2.1. Alkanes (paraffins): These molecules consist of carbon atoms which are all connected by single bonds and are saturated with hydrogen atoms (i.e. no mo ...
... Before learning how hydrocarbons react with oxygen in flames, we must first go over some nomenclature for the different classes of hydrocarbons. 2.1. Alkanes (paraffins): These molecules consist of carbon atoms which are all connected by single bonds and are saturated with hydrogen atoms (i.e. no mo ...
main types and mechanisms of the reactions in organic chemistry
... elimination is formed. Product of reaction is secondary propanol (propan-2-ol). In hydration reaction proton attaches in accordance with Markovnikov’s rule – to the carbon atom with more hydrogen atoms, as electron dencity shifts to this atom because of positive inductive effect of СН3-group. Beside ...
... elimination is formed. Product of reaction is secondary propanol (propan-2-ol). In hydration reaction proton attaches in accordance with Markovnikov’s rule – to the carbon atom with more hydrogen atoms, as electron dencity shifts to this atom because of positive inductive effect of СН3-group. Beside ...
PP IR Spectroscopy
... Infra-red spectra are complex due to the many different vibrations taking place in each molecule. Total characterisation of a substance based only on its IR spectrum is almost impossible unless one has computerised data handling facilities for comparison of the obtained spectrum with one in memory. ...
... Infra-red spectra are complex due to the many different vibrations taking place in each molecule. Total characterisation of a substance based only on its IR spectrum is almost impossible unless one has computerised data handling facilities for comparison of the obtained spectrum with one in memory. ...
Handout
... CH3CH2CH2CH2-, nbutyl (CH3)2CHCH2-, isobutyl CH3CH2CH(CH3)-, sbutyl (CH3)3C-, t-butyl ...
... CH3CH2CH2CH2-, nbutyl (CH3)2CHCH2-, isobutyl CH3CH2CH(CH3)-, sbutyl (CH3)3C-, t-butyl ...
PHASE TRANSFER CATALYSIS IN PHARMACEUTICAL
... alkylation of a large variety of organic anions derived from OH, NH, SH etc. acids, and particularly of carbanions of nitriles, esters, ketones, sulfones, acidic hydrocarbons and many others. For hydrolyzable compounds of higher CH acidity such as alkyl cyanoacetates, malonates, acetoacetates etc. l ...
... alkylation of a large variety of organic anions derived from OH, NH, SH etc. acids, and particularly of carbanions of nitriles, esters, ketones, sulfones, acidic hydrocarbons and many others. For hydrolyzable compounds of higher CH acidity such as alkyl cyanoacetates, malonates, acetoacetates etc. l ...
File - Chemistry Workshop
... A tertiary carbon is directly bonded to three other C’s. Multivalent atoms are 1º, 2º, or 3º by bonding to C’s. Univalent atom or group not really 1º, 2º, or 3º on its own - ID depends on type of carbon it is bonded to. ...
... A tertiary carbon is directly bonded to three other C’s. Multivalent atoms are 1º, 2º, or 3º by bonding to C’s. Univalent atom or group not really 1º, 2º, or 3º on its own - ID depends on type of carbon it is bonded to. ...
Ch25_outline-of-organic-nomenclature-1
... • Aromatic hydrocarbons are cyclic hydrocarbons that have some particular features. • There is a p-orbital on each atom. – The molecule is planar. ...
... • Aromatic hydrocarbons are cyclic hydrocarbons that have some particular features. • There is a p-orbital on each atom. – The molecule is planar. ...
Answers - Benjamin
... survive treatment with penicillin, and so develop at the expense of strains which are destroyed by penicillin. b The infection must be eradicated as far as possible, to prevent small numbers of mutants multiplying in an environment that gives them an advantage. ...
... survive treatment with penicillin, and so develop at the expense of strains which are destroyed by penicillin. b The infection must be eradicated as far as possible, to prevent small numbers of mutants multiplying in an environment that gives them an advantage. ...
Fall 2012
... 67. (11 pts) When 35.00 mL of 0.100 M HBr is added to 0. 275 g of strontium hydroxide in a calorimeter, 195.3 J of energy are released. What is the ΔH for this reaction? The balanced reaction is: Sr(OH)2 + 2 HBr ! SrBr2 + 2 H2O 68. (11 pts) One type of weather balloon has a volume limit of 2.00 x 10 ...
... 67. (11 pts) When 35.00 mL of 0.100 M HBr is added to 0. 275 g of strontium hydroxide in a calorimeter, 195.3 J of energy are released. What is the ΔH for this reaction? The balanced reaction is: Sr(OH)2 + 2 HBr ! SrBr2 + 2 H2O 68. (11 pts) One type of weather balloon has a volume limit of 2.00 x 10 ...
16A
... in liquid aldehydes and ketones, the intermolecular attractions are polar no hydrogen bonding is possible between aldehyde or ketone molecules aldehydes and ketones have lower boiling points than alcohols and carboxylic acids, compounds in which there is hydrogen ...
... in liquid aldehydes and ketones, the intermolecular attractions are polar no hydrogen bonding is possible between aldehyde or ketone molecules aldehydes and ketones have lower boiling points than alcohols and carboxylic acids, compounds in which there is hydrogen ...
Slides from Chapter 4 - FIU Faculty Websites
... 2. Number the parent to give the hydroxyl the lowest possible number" 3. The other substituents take their locations accordingly" ...
... 2. Number the parent to give the hydroxyl the lowest possible number" 3. The other substituents take their locations accordingly" ...
Chem 342 Jasperse Syllabus 1 Organic Chemistry II READING
... What’s Covered in Organic I versus Organic II differs between NDSU and MSUM The following are reading sections and problems associated with one chapter that was covered at MSUM in Organic I but is covered at NDSU in Organic II. Thus, if you are an NDSU student taking Organic II at MSUM, you will end ...
... What’s Covered in Organic I versus Organic II differs between NDSU and MSUM The following are reading sections and problems associated with one chapter that was covered at MSUM in Organic I but is covered at NDSU in Organic II. Thus, if you are an NDSU student taking Organic II at MSUM, you will end ...
EXPERIMENT 6: Reactions of Carbonyl Compounds: Qualitative
... cleavage that produce the haloform and the corresponding carboxylic acid. This is due to the weakened bond that only results when three halogens are attached to the carbon (making it a sufficient leaving group). Methyl secondary alcohols (-CHOHCH3) are also easily oxidized to their respective carbon ...
... cleavage that produce the haloform and the corresponding carboxylic acid. This is due to the weakened bond that only results when three halogens are attached to the carbon (making it a sufficient leaving group). Methyl secondary alcohols (-CHOHCH3) are also easily oxidized to their respective carbon ...
Alkene
In organic chemistry, an alkene is an unsaturated hydrocarbon that contains at least one carbon–carbon double bond. Alkene, olefin, and olefine are used often interchangeably (see nomenclature section below). Acyclic alkenes, with only one double bond and no other functional groups, known as mono-enes, form a homologous series of hydrocarbons with the general formula CnH2n. Alkenes have two hydrogen atoms less than the corresponding alkane (with the same number of carbon atoms). The simplest alkene, ethylene (C2H4), which has the International Union of Pure and Applied Chemistry (IUPAC) name ethene is the organic compound produced on the largest scale industrially. Aromatic compounds are often drawn as cyclic alkenes, but their structure and properties are different and they are not considered to be alkenes.