attack under the given reaction conditions? arbon is most likely to undergo a nucleophilic 1)CH₂CH₂MgBr 2) HO II (A) II is more likely to be attacked because it has a larger partial positive charge. (B) I is more likely to be attacked because it has a larger partial positive charge. (C) II is more likely to be attacked because it has less steric hindrance. (D) I is more likely to be attacked because it has less steric hindrance.

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter13: Substitution
Section: Chapter Questions
Problem 8CTQ
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attack under the given reaction conditions?
carbon is most likely to undergo a nucleophilic
(A) II is more likely to be attacked because it has a
larger partial positive charge.
(B) I is more likely to be attacked because it has a
larger partial positive charge.
*****
(C) II is more likely to be attacked because it has less
steric hindrance.
(A)
(D) I is more likely to be attacked because it has less
steric hindrance.
47. Which alkene will generate the product of this reaction
sequence?
(C)
?
1.
1) CH₂CH₂MgBr
2) H
O
R O H
2.00
CN
OH
(B)
(D)
K
48. Which are possible enol tautomers of
7-methyl-3-pentanone?
HO
Et
겨
Et
racemic
OH
H
CN
OH
Transcribed Image Text:attack under the given reaction conditions? carbon is most likely to undergo a nucleophilic (A) II is more likely to be attacked because it has a larger partial positive charge. (B) I is more likely to be attacked because it has a larger partial positive charge. ***** (C) II is more likely to be attacked because it has less steric hindrance. (A) (D) I is more likely to be attacked because it has less steric hindrance. 47. Which alkene will generate the product of this reaction sequence? (C) ? 1. 1) CH₂CH₂MgBr 2) H O R O H 2.00 CN OH (B) (D) K 48. Which are possible enol tautomers of 7-methyl-3-pentanone? HO Et 겨 Et racemic OH H CN OH
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