Organic Chemistry (6th Edition)
6th Edition
ISBN: 9781260119107
Author: Janice Gorzynski Smith
Publisher: McGraw Hill Education
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Textbook Question
Chapter 20, Problem 35P
Give the structure corresponding to each name.
a. cyclohexyl propanoate
b. cyclohexanecarboxamide
c.
d. Vinyl acetate
e. Benzoic propanoic anhydride
f.
g. octyl butanoate
h. N, N-dibenzylformamide
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Draw the structure corresponding to each name. a. 2-hydroxyheptanoic acid b. 4-chlorononanoic acid c. 3,4-dibromobenzoic acid d. lithium propanoate e. 2,2-dibromobutanoic acid f. ethyl 2-methylpropanoate
Give the structure corresponding to each name.a. cyclohexyl propanoateb. cyclohexanecarboxamidec. 4-methylheptanenitriled. vinyl acetatee. benzoic propanoic anhydridef. 3-methylhexanoyl chlorideg. octyl butanoateh. N,N-dibenzylformamide
Draw the structure corresponding to each name.
a. 3,3-dimethylpentanoic acid
b. 4-chloro-3-phenylheptanoic acid
c. (2R)-2-chloropropanoic acid
d. B,B-dichloropropionic acid
e. m-hydroxybenzoic acid
f. o-chlorobenzoic acid
i. 2,2-dichloropentanedioic acid
j. 4-isopropyl-2-methyloctanedioic acid
g. potassium acetate
h. sodium a-bromobutyrate
Chapter 20 Solutions
Organic Chemistry (6th Edition)
Ch. 20.1 - Prob. 1PCh. 20.2 - Draw the three possible resonance structures for...Ch. 20.2 - Prob. 3PCh. 20.3 - Give an IUPAC or common name for each compound. a....Ch. 20.3 - Problem 22.5 Draw the structure corresponding to...Ch. 20.4 - Problem 22.6 Explain why the boiling point of is...Ch. 20.7 - Prob. 11PCh. 20.7 - Prob. 12PCh. 20.8 - Prob. 13PCh. 20.9 - Problem 22.16 Draw the products of each reaction.
...
Ch. 20.9 - Prob. 17PCh. 20.9 - Problem 22.18 Draw a stepwise mechanism for the...Ch. 20.9 - Prob. 19PCh. 20.10 - Problem 22.20 Fenofibrate is a...Ch. 20.10 - Problem 22.21 What product is formed when the...Ch. 20 - Prob. 33PCh. 20 - 22.40 Give the IUPAC or common name for each...Ch. 20 - 22.41 Give the structure corresponding to each...Ch. 20 - Prob. 36PCh. 20 - 22.43 Explain why is a stronger acid and a weaker...Ch. 20 - (a) Propose an explanation for the difference in...Ch. 20 - Draw the product formed when phenylacetic acid is...Ch. 20 - Prob. 42PCh. 20 - Prob. 43PCh. 20 - Prob. 44PCh. 20 - Prob. 45PCh. 20 - Prob. 46PCh. 20 - Prob. 47PCh. 20 - Prob. 48PCh. 20 - 22.64 What carboxylic acid and alcohol are needed...Ch. 20 - Problem 22.65 Devise a synthesis of each compound...Ch. 20 - 22.70 What polyester or poly amide can be prepared...Ch. 20 - 22.71 What two monomers are needed to prepare each...
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- Draw the structure corresponding to each name. a. 1-decanamine b. tricyclohexylamine c. p-bromoaniline d. 3-aminobutanoic acid e. N,N-dipropyl-2-octanamine f. N-ethylhexylaminearrow_forwardCyclopentanone is treated with chlorine (Cl2) in the presence of acid (H*). What product is formed? A. Chlorocyclopentane B. 1-chloro-1-hydroxycyclopentane C. 2-chlorocyclopentanone D. 3-chlorocyclopentanonearrow_forwardReduction of an alkyl azide results in the formation of —-. A. an imine B. an oxime C. a tertiary amine D. a secondary amine E. a primary aminearrow_forward
- 1. An alkene reacts with water with an acid catalyst results into a formation of: A. Aldehyde B. Ketone C. Alcohol D. Ester 2. 3-Methylhexanal with K2Cr2O7 will yield: A. 3-Methyl-1-hexanol B. 3-Methylhexanoic acid C. 3-Methyl-1-hexanone D. 3-Methyl-1-hexanethiol 3. This is a reverse process of Hydration reaction: A. Oxidation reaction B. Reduction reaction C. Dehydration reaction D. Hydration reaction 4. Acetic acid reacts with a strong base forms: A. Salt B. Water C. Salt and Water D. No reaction 5. Ketones can be further oxidized with benedict's solution into: A. Alcohol B. Aldehyde C. Catalysts D. No reactionarrow_forward1. Cite some reactions in which formaldehyde behaves differently from other aldehydes. 2. Give some biological and medical applications of: a. formalin b. chloral c. urotropinearrow_forwardон C-H ÓR Compound that contains a group like that shown above. a. acetal Ob. aldehyde c. Benedict's reagent d. carbonyl Oe. hemiacetal Of. hemiketal Og. hydrolysis h. ketal i. ketone Oj. Tollen's reagent 2.arrow_forward
- 1. Give the structure corresponding to each name. a. 4-ethyl-3-heptanol b. 3-chloro-1,2-propanediol c. diisobutyl ether d. 1,2-epoxy-1,3,3-trimethylcyclohexane e. 1-ethoxy-3-ethylheptanearrow_forward1. Which carbonyl group of the given compound is most reactive for nucleophilic addition reaction? a. All have equal reactivity b. Carbonyl Group 1 c. Carbonyl Group 2 d. Carbonyl Group 2. An aldehyde commonly exhibits a nucleophilic addition type of reaction. When a nucleophile attacks a carbonyl carbon, what happens to the oxygen atom in the structure? Refer to the structure below. ~ a. Oxygen atom becomes more electronegative. b. Oxygen atom obtains a net negative charge. c. Oxygen atom transforms to an alkoxide group. d. Oxygen atom acts as the new electrophile. 3. Assign the trivial name of the structure below. a. Diphenylketone b. Benzyl phenylketone c. Diphenyl aldehyde d. Benzyl phenyl aldehydearrow_forward2. Draw out the following compounds. a. N-methylaniline b. Triisopropylamine c. N,N-dipropylhexylamine d. 1,5-pentanediamine (Also known as Cadaverine for its smell)arrow_forward
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