Considering the retrosynthetic analysis to make target molecule, X, which of the following starting reactants cannot be used to accomplish the synthesis of X in a single reaction? Starting reactants Target molecule X A) A B) B T A C) C Which of the following circled budmonas in B D) more than one of these с E) none of these

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Considering the retrosynthetic analysis to make target molecule, X, which of the following starting
reactants cannot be used to accomplish the synthesis of X in a single reaction?
Starting reactants
Target molecule X
A) A
H
H-CH
H
I
B) B
A)
Which of the following circled hydrogens is the most acidic?
H
CH₂
H
H₂C-C-H
H₂C-CH
CH₂
CH₂
11
111
D. (E)-pent-2-ene
E. (Z)-pent-2-ene
A
C) C
B)
a. carbanion
e. none of the above
D) more than one of these
H₂C=C
C)
A) oct-1-ene B) (E)-oct-2-ene
B
H
IV
Compound B has a molecular formula of C6H12. It reacts with hot, concentrated KMnO4 to produce
two identical molecules. The major product of oxidative cleavage by ozonolysis is identical to the
major product by reaction with permanganate. What is a possible structure of compound B?
H₂C-CECH
Which of the molecules listed below has the highest boiling point?
A. 2-methylbut-2-ene
B. 2-methylpent-2-ene
C. (E)-but-2-ene
c. free radical
more than
one of
these
VA
D)
target molecule
C
6. Which of the following intermediates is thought to occur in the mechanism by which alkenes are
hydrated in the presence of acid?
b. carbocation
E) none of these
C) (Z)-oct-2-ene
none of
these
E)
Which of the following would be the best alkene to use in a reaction with water in the presence of
catalytic H₂SO4 to make the target molecule in the highest percentage yield?
OH
d. mercurinium ion
D) either B or C
E) none of these
Transcribed Image Text:Considering the retrosynthetic analysis to make target molecule, X, which of the following starting reactants cannot be used to accomplish the synthesis of X in a single reaction? Starting reactants Target molecule X A) A H H-CH H I B) B A) Which of the following circled hydrogens is the most acidic? H CH₂ H H₂C-C-H H₂C-CH CH₂ CH₂ 11 111 D. (E)-pent-2-ene E. (Z)-pent-2-ene A C) C B) a. carbanion e. none of the above D) more than one of these H₂C=C C) A) oct-1-ene B) (E)-oct-2-ene B H IV Compound B has a molecular formula of C6H12. It reacts with hot, concentrated KMnO4 to produce two identical molecules. The major product of oxidative cleavage by ozonolysis is identical to the major product by reaction with permanganate. What is a possible structure of compound B? H₂C-CECH Which of the molecules listed below has the highest boiling point? A. 2-methylbut-2-ene B. 2-methylpent-2-ene C. (E)-but-2-ene c. free radical more than one of these VA D) target molecule C 6. Which of the following intermediates is thought to occur in the mechanism by which alkenes are hydrated in the presence of acid? b. carbocation E) none of these C) (Z)-oct-2-ene none of these E) Which of the following would be the best alkene to use in a reaction with water in the presence of catalytic H₂SO4 to make the target molecule in the highest percentage yield? OH d. mercurinium ion D) either B or C E) none of these
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