ll mobily ?4:13 PMO 21% O< Homework - carboxylic a...CH3CHCH2CH2CHCH3CH3CCO2HCH3(c).CO2H(d)CH3CH3CCNCH3(g)Br(h)CNBRCH2CHCH2CH2CO2HQ2:Draw structures corresponding to the following IUPAC names:(a) cis-1,2-Cyclohexanedicarboxylic acid(b) Heptanedioic acid(c) 2-Hexen-4-ynoic acid(d) 4-Ethyl-2-propyloctanoic acid(e) 2-CyclobutenecarbonitrileQ3:How could you convert butanoic acid into the following compounds?Write each step showing the reagents needed.(a) 1-Butanol (b) 1-Bromobutane (c) 1-ButeneHow could you convert each of the following compounds into butanoicacid? Write each step showing all reagents.(a) 1-Butanol(b) 1-Bromobutane (c) 1-ButeneHow could you convert butanenitrile into the following compounds?Write each step showing the reagents needed.(a) 1-Butanol (b) Butylamine

Since you have asked multiple question, we will solve the first question for you. If you want any…

Q2: Draw structures corresponding to the following IUPAC names: (a) cis-1,2-Cyclohexanedicarboxylic acid (b) Heptanedioic acid (c) 2-Hexen-4-ynoic acid (d) 4-Ethyl-2-propyloctanoic acid (e) 2-Cyclobutenecarbonitrile

Q2: Draw structures corresponding to the following IUPAC names: (a) cis-1,2-Cyclohexanedicarboxylic acid (b) Heptanedioic acid (c) 2-Hexen-4-ynoic acid (d) 4-Ethyl-2-propyloctanoic acid (e) 2-Cyclobutenecarbonitrile

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter22: Carbonyl Alpha-substitution Reactions

Section22.SE: Something Extra

Problem 64AP: The key step in a reported laboratory synthesis of sativene, a hydrocarbon isolated from the mold...

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Question

ll mobily ?
4:13 PM
O 21% O
< Homework - carboxylic a...
CH3CHCH2CH2CHCH3
CH3CCO2H
CH3
(c)
.CO2H
(d)
CH3
CH3CCN
CH3
(g)
Br
(h)
CN
BRCH2CHCH2CH2CO2H
Q2:
Draw structures corresponding to the following IUPAC names:
(a) cis-1,2-Cyclohexanedicarboxylic acid
(b) Heptanedioic acid
(c) 2-Hexen-4-ynoic acid
(d) 4-Ethyl-2-propyloctanoic acid
(e) 2-Cyclobutenecarbonitrile
Q3:
How could you convert butanoic acid into the following compounds?
Write each step showing the reagents needed.
(a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene
How could you convert each of the following compounds into butanoic
acid? Write each step showing all reagents.
(a) 1-Butanol
(b) 1-Bromobutane (c) 1-Butene
How could you convert butanenitrile into the following compounds?
Write each step showing the reagents needed.
(a) 1-Butanol (b) Butylamine

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