[Answered] How many constitutional monochloride isomers will form in the radical-chain chlorination of ...

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asmith134

Hero Member
Posts: 576

on: Aug 23, 2018

How many constitutional monochloride isomers will form in the radical-chain chlorination of 2,3-dimethylpentane?
1.3
2.4
3.5
4.6
5.7

Question 2

Consider the carbocations shown below. Which carbocation is more stabilized and why?

1.The vinyl cation is more stabilized due to resonance.
2.The vinyl cation is more stabilized because it is a stronger Lewis acid.
3.The vinyl cation is more stabilized because of hyperconjugation.
4.The ethyl cation is more stabilized due to a C-H/p orbital interaction.
5.The ethyl cation is more stabilized due to a C-H/p orbital interaction.

Question 3

Which compound cannot serve as an immediate precursor to the synthetic target shown below?

Question 4

What is the structure of intermediate I?

Question 5

A reaction of propyne with Hg2+ is run in methanol (CH3OH) in the absence of water, but in the presence of a strong acid (H+) with a non-nucleophilic counterion. If this reaction follows a typical mechanism of electrophilic addition, what would be the expected product?

Question 6

2-Butyne is allowed to react with H2 over the Lindlar catalysts. The obtained product is treated with OsO4/pyridine followed by NaHSO3/H2O. Which of the following compounds is the end result of this sequence of reactions?

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Marked as best answer by a Subject Expert

cclemon1

Sr. Member
Posts: 312

Reply #1 on: Aug 23, 2018

Answer to Question 1

4

Answer to Question 2

5

Answer to Question 3

1

Answer to Question 4

5

Answer to Question 5

3

Answer to Question 6

5

Answer to Question 7

5

asmith134

Member
Posts: 576

Reply 2 on: Aug 23, 2018

TYSM

Member
Posts:

Reply 3 on: Yesterday

Great answer, keep it coming

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