CNCT ORG CHEM 6 2020
6th Edition
ISBN: 9781266807244
Author: SMITH
Publisher: MCG
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Textbook Question
Chapter 3, Problem 35P
Identify each
represents a lactone-a cyclic ester- and which represents a lactam-a cyclic amide?
a. 
b. 
c. 
d. 
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17. Which functional groups are in the following molecule of aspirin?
HO,
a benzene ring, an ester, a ketone, and an alcohol
b. a benzene ring, two ketones, an ether, and an alcohol
a benzene ring, a carboxylic acid, an ether, and a ketone
d. a benzene ring, a carboxylic acid, and an ester
a.
c.
The hydrolysis of an amide in acidic conditions forms
A. a carboxylate salt and an alcohol
B. a carboxylate salt and an amine
C. an alcohol and an amine salt (an ammonium ion)
D. a carboxylic acid and an amine salt (an ammonium ion)
Jj.166.
Draw each amide. N-butyl-N-methylbenzamide
Chapter 3 Solutions
CNCT ORG CHEM 6 2020
Ch. 3.1 - Prob. 1PCh. 3.2 - (a) Classify the carbon atoms in each compound as...Ch. 3.2 - Problem 3.3 Classify a carbon atom by the number...Ch. 3.2 - Classify each alkyl halide and alcohol as , or...Ch. 3.2 - Prob. 5PCh. 3.2 - Prob. 6PCh. 3.2 - Draw the structure of a compound of molecular...Ch. 3.2 - Prob. 8PCh. 3.2 - Prob. 9PCh. 3.2 - Draw the structure of a compound fitting each...
Ch. 3.4 - Predict which compound in each pair has the higher...Ch. 3.4 - Prob. 17PCh. 3.4 - a Label the hydrophobic and hydrophilic portions...Ch. 3.5 - Prob. 21PCh. 3 - 3.29
Identify the functional groups in the...Ch. 3 - Prob. 32PCh. 3 - 3.31 For each alkane: (a) classify each carbon...Ch. 3 - 3.32 Identify the functional groups in each...Ch. 3 - 3.33 Identify each functional group located in the...Ch. 3 - 3.34 (a)Identify the functional groups in...Ch. 3 - Draw seven constitutional isomers with molecular...Ch. 3 - Prob. 38PCh. 3 - Prob. 39PCh. 3 - Prob. 40PCh. 3 - Intramolecular force of attraction are often...Ch. 3 - 3.40 (a) Draw four compounds with molecular...Ch. 3 - 3.41 Rank the compounds in each group in order of...Ch. 3 - Explain why CH3CH2NHCH3 has higher boiling point...Ch. 3 - Prob. 45PCh. 3 - 3.44 Rank the following compounds in order of...Ch. 3 - Prob. 47PCh. 3 - 3.50 Predict the solubility of each of the...Ch. 3 - Prob. 52PCh. 3 - Prob. 53PCh. 3 - 3.53 THC is the active component in marijuana, and...Ch. 3 - Prob. 55PCh. 3 - Prob. 56PCh. 3 - 3.60 Quinapril (trade name Accupril) is a drug...Ch. 3 - 3.61 Answer each question about oxycodone, a...Ch. 3 - Prob. 65PCh. 3 - Prob. 66PCh. 3 - 3.64 Explain why A is less water soluble than B,...Ch. 3 - 3.65 Recall from section 1.10B that there is...
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- What amine is formed by reduction of each amide?arrow_forwardDraw a structural formula for each amine and amine derivative. Q.) trans-2-Aminocyclohexanolarrow_forward1. Which statement best described the ability of amines to hydrogen bond? A. Primary, secondary and tertiary amines can all hydrogen bond with molecules identical to themselves. B. Primary and secondary amines can hydrogen bond with molecules identical to themselves, but tertiary amines cannot. C. Only primary amines can hydrogen bond with molecules identical to themselves. Secondary and tertiary amines cannot. D. Primary, secondary and tertiary amines cannot hydrogen bond with molecules identical to themselves, but the can hydrogen bond with water.arrow_forward
- amine, (2) an amide, or (3) both an amine and an amide. 17-106 Classify each of the following compounds as (1) an amine, (2) an amide, or (3) both an amine and an NH2 b. `NH a. H2N H d. с.arrow_forwardErythronolide B is the biological precursor of erythromycin, a broad-spectrum antibiotic. What functional group Erythronolide B does contain? a. b. H₂CH₂C C. H₂C 1 H₂C 2 3 4 O Amide d. Amine OH Erythronolide B Ketone Aldehyde a CH₂ b C d CH₂ OH JCH₂ 'OH OHarrow_forwardDraw a structural formula for each amine and amine derivative. Q.) Benzylaminearrow_forward
- Identify the functional groups in the two molecules shown below. Then, for each ester or amide functional group, write a reaction showing how the molecule could be made. H. H.arrow_forwardWhat are the functional groups present in this antibacterial antibiotic? A. Nitro, phenyl, amine, carbonyl, hydroxyl B. Nitro, phenyl, amine, carbonyl, C. Nitro, phenyl, amine, hydroxyl D. Nitro, phenol, amine, carbonyl, hydroxyl A brief explanation would be highly appreciated + upvotearrow_forwardDraw a structural formula for each amine and amine derivative. Q.)1-Phenyl-2-propanamine (amphetamine)arrow_forward
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