- Consider the reaction below to answer the following questions: S Write the complete stepwise mechanism for this reaction. Show intermediate structures and electron flow with arrows. OEt -ОН но- This reaction is an example of: a. an intermolecular aldol reaction b. an intramolecular aldol reaction C. a mixed aldol reaction d. Michael reaction e. Stork reaction + H₂O + EtO- The purpose of the base catalyst in this reaction is: a. to polarize the carbonyl group to make it more electrophilic b. to convert the ester to an intermediate carboxylic acid C. to convert the alcohol group to an alkoxide anion, which is a better nucleophile d. to convert the alcohol group to an alkoxide anion, which is a better electrophile all of the above e.

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Chapter1: Chemical Foundations
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6.
Consider the reaction below to answer the following questions:
OEt
-OH
HO-
This reaction is an example of:
a.
an intermolecular aldol reaction
b. an intramolecular aldol reaction
a mixed aldol reaction
C.
d. Michael reaction
e.
Stork reaction
+ H₂O
Write the complete stepwise mechanism for this reaction. Show intermediate structures and all
electron flow with arrows.
+
EtO-
The purpose of the base catalyst in this reaction is:
a. to polarize the carbonyl group to make it more electrophilic
b. to convert the ester to an intermediate carboxylic acid
C.
to convert the alcohol group to an alkoxide anion, which is a better nucleophile
d. to convert the alcohol group to an alkoxide anion, which is a better electrophile
e. all of the above
Transcribed Image Text:6. Consider the reaction below to answer the following questions: OEt -OH HO- This reaction is an example of: a. an intermolecular aldol reaction b. an intramolecular aldol reaction a mixed aldol reaction C. d. Michael reaction e. Stork reaction + H₂O Write the complete stepwise mechanism for this reaction. Show intermediate structures and all electron flow with arrows. + EtO- The purpose of the base catalyst in this reaction is: a. to polarize the carbonyl group to make it more electrophilic b. to convert the ester to an intermediate carboxylic acid C. to convert the alcohol group to an alkoxide anion, which is a better nucleophile d. to convert the alcohol group to an alkoxide anion, which is a better electrophile e. all of the above
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