This topic contains a solution. Click here to go to the answer

Author Question: Instructions: Draw the structure of the major organic products(s) for each of the following ... (Read 33 times)

LCritchfi

  • Hero Member
  • *****
  • Posts: 519
Instructions:
   
  Draw the structure of the major organic products(s) for each of the following reactions. Indicate the stereochemistry for each reaction when appropriate.
 

Question 2

Instructions:
   
  Draw the structure of the major organic products(s) for each of the following reactions. Indicate the stereochemistry for each reaction when appropriate.
 

Question 3

Instructions:
   
  Draw the structure of the major organic products(s) for each of the following reactions. Indicate the stereochemistry for each reaction when appropriate.
 

Question 4

Instructions:
   
  Draw the structure of the major organic products(s) for each of the following reactions. Indicate the stereochemistry for each reaction when appropriate.
 

Question 5

Instructions:
   
  Draw the structure of the major organic products(s) for each of the following reactions. Indicate the stereochemistry for each reaction when appropriate.
 

Question 6

Instructions:
   
  Draw the structure of the major organic products(s) for each of the following reactions. Indicate the stereochemistry for each reaction when appropriate.
 

Question 7

Consider the reactions below to answer the following questions.
   
 
  Halving the concentration of hydroxide in these reactions:
   
  a.
  causes the reaction mechanism to change
  b.
  halves the rate of reaction
  c.
  has no effect on the rate of reaction
  d.
  doubles the rate of reaction

Question 8

Consider the reactions below to answer the following questions.
   
 
  The mechanism for these reactions is:
   
  a.
  SN1
  b.
  SN2
  c.
  E1
  d.
  E2

Question 9

Consider the reactions below to answer the following questions.
   
 
  Which reaction would be predicted to be faster? Explain.

Question 10

Draw all the monochlorination products of methylcyclopentane (ignore stereoisomers).

Question 11

Consider the following reaction:
   
 
   
  a)
  Draw the product of the reaction. How would you categorize this process mechanistically?
   
   
  b)
  Which of the following spectral methods could be used to follow the progress of the reaction?
   
  a. NMR spectroscopy
   
  b. Mass spectrometry
   
  c. Infrared spectroscopy
   
  d. UV spectroscopy
   
  e. all of these
   
  f. a, b, and c only

Question 12

Predict the product of the following reaction:
   
 

Question 13

Which of the following represents the transition state of the SN2 reaction between methyl iodide and ammonia?
  a.
 
   
  b.
 
   
  c.
 
   
  d.
 

Question 14

What is the IUPAC name of the following compound?
   
 
   
  a.
  (R)-2-bromo-2-vinylpentane
  b.
  (S)-2-bromo-2-vinylpentane
  c.
  (S)-3-bromo-3-propylbut-1-ene
  d.
  (R)-3-bromo-3-methylhex-1-ene

Question 15

Consider the following compound:
   
 
   
  a)
  What is the IUPAC name of the compound?
   
  a. (R)-1-chloro-3-methyl-2-cyclohexene
   
  b. (S)-1-chloro-3-methyl-2-cyclohexene
   
  c. (R)-3-chloro-1-methylcyclohexene
   
  d. (S)-3-chloro-1-methylcyclohexene
   
   
  b)
  How could this compound be used to produce a conjugated diene?
   
  a. substitution
   
  b. elimination
   
  c. allylic free radical formation
   
  d. either b or c

Question 16

What is the rate law for the E2 reaction of an alkyl halide (RX) with sodium ethoxide (NaOEt) in ethanol solvent (EtOH)?
  a.
  rate = kRX
  b.
  rate = kRX2
  c.
  rate = kRXNa+
  d.
  rate = kRXOEt-
  e.
  rate = kOEt-

Question 17

Which mechanism is favored by the reaction of a secondary alkyl bromide with potassium t-butoxide?
  a.
  SN1
  b.
  SN2
  c.
  E1
  d.
  E1CB
  e.
  E2



Related Topics

Need homework help now?

Ask unlimited questions for free

Ask a Question
Marked as best answer by a Subject Expert

cassie_ragen

  • Sr. Member
  • ****
  • Posts: 347
Answer to Question 1



Answer to Question 2



Answer to Question 3



Answer to Question 4



Answer to Question 5



Answer to Question 6



Answer to Question 7

b

Answer to Question 8

b

Answer to Question 9

ANS: Reaction b. is faster because -I is a better leaving group than -F.

Answer to Question 10



Answer to Question 11

a)


This is an E1CB reaction.

b)
e

Consider the reaction below to answer the following questions.



Answer to Question 12



Answer to Question 13

c

Answer to Question 14

d

Answer to Question 15

ANS:
a)
c

b)
d

Answer to Question 16

d

Answer to Question 17

e




LCritchfi

  • Member
  • Posts: 519
Reply 2 on: Aug 23, 2018
Great answer, keep it coming :)


jomama

  • Member
  • Posts: 346
Reply 3 on: Yesterday
YES! Correct, THANKS for helping me on my review

 

Did you know?

Drug abusers experience the following scenario: The pleasure given by their drug (or drugs) of choice is so strong that it is difficult to eradicate even after years of staying away from the substances involved. Certain triggers may cause a drug abuser to relapse. Research shows that long-term drug abuse results in significant changes in brain function that persist long after an individual stops using drugs. It is most important to realize that the same is true of not just illegal substances but alcohol and tobacco as well.

Did you know?

After a vasectomy, it takes about 12 ejaculations to clear out sperm that were already beyond the blocked area.

Did you know?

The word drug comes from the Dutch word droog (meaning "dry"). For centuries, most drugs came from dried plants, hence the name.

Did you know?

The liver is the only organ that has the ability to regenerate itself after certain types of damage. As much as 25% of the liver can be removed, and it will still regenerate back to its original shape and size. However, the liver cannot regenerate after severe damage caused by alcohol.

Did you know?

People about to have surgery must tell their health care providers about all supplements they take.

For a complete list of videos, visit our video library