[References] From the table of available reagents select the one(s) you would use to convert cyclohexanone to the following compound: CH,CH,CO,H Use the minimum number of steps; from one to five are required. List reagents by letter in the order that they are used; example: fa. Submit Answer Reagents Available a. BH3, THF; followed by H₂O2, "OH b. Br₂, CH3CO₂H c. HCN, KCN d. H₂O*, heat e. LDA (lithium diisopropylamide) f. NaBH4 Try Another Version g. Na "CH(CO₂C₂H5) (from CH₂(CO₂C₂H5)2 + Na* -OC₂H5) h. PBr3 i. PhCH₂Br j. Ph3P+--CH₂ k. pyridine, heat I. PhBr 10 item attempts remaining
[References] From the table of available reagents select the one(s) you would use to convert cyclohexanone to the following compound: CH,CH,CO,H Use the minimum number of steps; from one to five are required. List reagents by letter in the order that they are used; example: fa. Submit Answer Reagents Available a. BH3, THF; followed by H₂O2, "OH b. Br₂, CH3CO₂H c. HCN, KCN d. H₂O*, heat e. LDA (lithium diisopropylamide) f. NaBH4 Try Another Version g. Na "CH(CO₂C₂H5) (from CH₂(CO₂C₂H5)2 + Na* -OC₂H5) h. PBr3 i. PhCH₂Br j. Ph3P+--CH₂ k. pyridine, heat I. PhBr 10 item attempts remaining
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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Select the reagent(s) below to convert cyclohexanone to the following compound
![**Cyclohexanone Conversion Exercise**
From the table of available reagents, select the one(s) you would use to convert cyclohexanone to the following compound:
![Chemical Structure: Cyclohexanone is depicted as a hexagonal ring structure with a CH₂CH₂CO₂H substituent.]
**Instructions:**
- Use the minimum number of steps; from one to five are required.
- List reagents by letter in the order that they are used; example: fa.
**Reagents Available:**
a. BH₃, THF; followed by H₂O₂, `OH`
b. Br₂, CH₃CO₂H
c. HCN, KCN
d. H₃O⁺, heat
e. LDA (lithium diisopropylamide)
f. NaBH₄
g. Na⁺CH(CO₂C₂H₅)₂ (from CH₂(CO₂C₂H₅)₂ + Na⁺ -OC₂H₅)
h. PBr₃
i. PhCH₂Br
j. Ph₃P⁺-CH₂
k. Pyridine, heat
l. PhBr
[Submit Answer] [Try Another Version]
*10 item attempts remaining*
This exercise involves selecting the correct reagents and steps in an organic chemistry reaction to achieve the desired transformation.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F529b86fd-80df-416e-a592-e1d0472fa200%2F1b4b0677-b275-4d01-8d05-ab50b868f9fb%2Fykheh1_processed.jpeg&w=3840&q=75)
Transcribed Image Text:**Cyclohexanone Conversion Exercise**
From the table of available reagents, select the one(s) you would use to convert cyclohexanone to the following compound:
![Chemical Structure: Cyclohexanone is depicted as a hexagonal ring structure with a CH₂CH₂CO₂H substituent.]
**Instructions:**
- Use the minimum number of steps; from one to five are required.
- List reagents by letter in the order that they are used; example: fa.
**Reagents Available:**
a. BH₃, THF; followed by H₂O₂, `OH`
b. Br₂, CH₃CO₂H
c. HCN, KCN
d. H₃O⁺, heat
e. LDA (lithium diisopropylamide)
f. NaBH₄
g. Na⁺CH(CO₂C₂H₅)₂ (from CH₂(CO₂C₂H₅)₂ + Na⁺ -OC₂H₅)
h. PBr₃
i. PhCH₂Br
j. Ph₃P⁺-CH₂
k. Pyridine, heat
l. PhBr
[Submit Answer] [Try Another Version]
*10 item attempts remaining*
This exercise involves selecting the correct reagents and steps in an organic chemistry reaction to achieve the desired transformation.
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