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Author Question: How many constitutional monochloride isomers will form in the radical-chain chlorination of ... (Read 60 times)

asmith134

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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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cclemon1

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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
Excellent

nguyenhoanhat

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Reply 3 on: Yesterday
YES! Correct, THANKS for helping me on my review

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