b. Discuss the mechanism for any two of the reactions shown in Figure 4. Include all curly arrows, as well as any relevant stereochemistry considerations in your answer. Ян (i) (ii) (iii) Ph Br iOH OH NaCN HCI MeOH HO NEt3 C4H₂NO + NaCl A C8H₂O2 + B H₂SO4 catalyst Figure 4 e Br HNE13 C7H1402 + H₂O C
b. Discuss the mechanism for any two of the reactions shown in Figure 4. Include all curly arrows, as well as any relevant stereochemistry considerations in your answer. Ян (i) (ii) (iii) Ph Br iOH OH NaCN HCI MeOH HO NEt3 C4H₂NO + NaCl A C8H₂O2 + B H₂SO4 catalyst Figure 4 e Br HNE13 C7H1402 + H₂O C
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Chapter1: Chemical Foundations
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Transcribed Image Text:b.
Discuss the mechanism for any two of the reactions shown in Figure 4. Include
all curly arrows, as well as any relevant stereochemistry considerations in your
answer.
Ян
(i)
(ii)
(iii)
Ph Br
iOH
OH
NaCN
HCI
MeOH
HO
NEt3
C4H₂NO + NaCl
A
C8H₂O2 +
B
H₂SO4 catalyst
Figure 4
e
Br
HNE13
C7H1402 + H₂O
C
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VIEWStep 2: A) Propanal reacting with NaCN in HCl to give propylcyanihydrine
VIEWStep 3: B) Phenylbromide reacting with methanol using triethylamine to give ester formation (methyl phenyl e
VIEWStep 4: C) Ethanoic acid reacting with 4-methylpentanol to give ester formation:
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