16.32 Draw structures corresponding to the following names: (a) p-Bromophenylacetamide (b) m-Benzoylbenzamide (c) 2,2-Dimethylhexanamide (d) Cyclohexyl cyclohexanecarboxylate (e) Ethyl cyclobut-2-enecarboxylate (f) Succinic anhydride
16.32 Draw structures corresponding to the following names: (a) p-Bromophenylacetamide (b) m-Benzoylbenzamide (c) 2,2-Dimethylhexanamide (d) Cyclohexyl cyclohexanecarboxylate (e) Ethyl cyclobut-2-enecarboxylate (f) Succinic anhydride
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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![16.33 Draw and name compounds that meet the following descriptions:
(a) Three thioesters having the formula CgH10OS
(b) Three amides having the formula C,H11NO](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Ff0f33436-83c8-4223-ad35-da8643a4fe85%2Fdd4059d9-8826-42a6-b6df-554463df8389%2F2v92j3a_processed.png&w=3840&q=75)
Transcribed Image Text:16.33 Draw and name compounds that meet the following descriptions:
(a) Three thioesters having the formula CgH10OS
(b) Three amides having the formula C,H11NO
![Naming Carboxylic Acid Derivatives
16.31 Give IUPAC names for the following compounds:
(a)
(b)
CH2CH3 0
le)
CH,CH,CHCH=CHCI
CI
CH3OČCH,CH,COCH3
“NH2
H3C-
(d)
le)
(f)
CH,CH,COCHCH3
CH3CHCH,ČNHCH3
.cOCH3
Br
(g)
(h)
SCHICH3)2
16.32 Draw structures corresponding to the following names:
(a) p-Bromophenylacetamide
(b) m-Benzoylbenzamide
(c) 2,2-Dimethylhexanamide
(d) Cyclohexyl cyclohexanecarboxylate
(e) Ethyl cyclobut-2-enecarboxylate
(f) Succinic anhydride](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Ff0f33436-83c8-4223-ad35-da8643a4fe85%2Fdd4059d9-8826-42a6-b6df-554463df8389%2Ft0c2u2_processed.png&w=3840&q=75)
Transcribed Image Text:Naming Carboxylic Acid Derivatives
16.31 Give IUPAC names for the following compounds:
(a)
(b)
CH2CH3 0
le)
CH,CH,CHCH=CHCI
CI
CH3OČCH,CH,COCH3
“NH2
H3C-
(d)
le)
(f)
CH,CH,COCHCH3
CH3CHCH,ČNHCH3
.cOCH3
Br
(g)
(h)
SCHICH3)2
16.32 Draw structures corresponding to the following names:
(a) p-Bromophenylacetamide
(b) m-Benzoylbenzamide
(c) 2,2-Dimethylhexanamide
(d) Cyclohexyl cyclohexanecarboxylate
(e) Ethyl cyclobut-2-enecarboxylate
(f) Succinic anhydride
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