On the structures provided, draw arrows showing the electron flow ...

[Alainaaa8]

On the structures provided, draw arrows showing the electron flow in the reaction mechanism for the electrophilic addition of hydrogen bromide to hex-1-yne.
   
 

Question 2

Instructions: Predict the products of each reaction below. Indicate regiochemistry and stereochemistry when relevant.
  Predict and indicate.
   
 

Question 3

Instructions: Predict the products of each reaction below. Indicate regiochemistry and stereochemistry when relevant.
  Predict and indicate.
   
 

Question 4

Instructions: Predict the products of each reaction below. Indicate regiochemistry and stereochemistry when relevant.
  Predict and indicate.
   
 

Question 5

Instructions: Predict the products of each reaction below. Indicate regiochemistry and stereochemistry when relevant.
  Predict and indicate.
   
 

Question 6

Instructions: Predict the products of each reaction below. Indicate regiochemistry and stereochemistry when relevant.
  Predict and indicate.
   
 

Question 7

Instructions: Predict the products of each reaction below. Indicate regiochemistry and stereochemistry when relevant.
  Predict and indicate.
   
 

Question 8

Instructions: Predict the products of each reaction below. Indicate regiochemistry and stereochemistry when relevant.
  Predict and indicate.
   
 

Question 9

Instructions: Predict the products of each reaction below. Indicate regiochemistry and stereochemistry when relevant.
  Predict and indicate:
   
 

Question 10

Instructions: To answer the question(s) below, consider the following reaction:
   
  When cyclohexene reacts with chlorine in tetrachloromethane, the following dihalide is formed.
   
 
 
  Refer to instructions. Provide the IUPAC name for the product of this reaction.

Question 11

Instructions: To answer the question(s) below, consider the following reaction:
   
  When cyclohexene reacts with chlorine in tetrachloromethane, the following dihalide is formed.
   
 
  Refer to instructions. Since the two chlorine atoms add to opposite faces of the cyclohexene double bond, we say that the reaction occurs with:
   
  a. syn stereochemistry
  b. cis stereochemistry
  c. anti stereochemistry
  d. retention of stereochemistry

Question 12

Predict the major product of the following reaction.
   
 

Question 13

Instructions: The reaction of 2-methylpropene with HBr in ether gives one of the two products below. Answer the following question(s) about this reaction.
   
 
  Refer to instructions. Which product is the Markovnikov product?

Question 14

Instructions: The reaction of 2-methylpropene with HBr in ether gives one of the two products below. Answer the following question(s) about this reaction.
   
 
  Refer to instructions. The reaction mixture would contain a majority of which isomeric product?

Question 15

The product(s) of the reaction when carried out in an organic solvent
   
 
   
  would be:
  a.
  cis-1,2-dibromocyclohexane only
  b.
  trans-1,2-dibromocyclohexane only
  c.
  50/50 mixture of cis-1,2-dibromocyclohexane and trans-1,2-dibromocyclohexane only
  d.
  mixture with > 50 being trans-1,2-dibromocyclohexane only

Question 16

Instructions: Predict the structure of the alkene you would use to prepare the folloiwng compounds. There may be more than one answer in some cases.
  Predict.
   
 

Question 17

Instructions: Predict the structure of the alkene you would use to prepare the folloiwng compounds. There may be more than one answer in some cases.
  Predict.
   
 

Question 18

Instructions: Predict the structure of the alkene you would use to prepare the folloiwng compounds. There may be more than one answer in some cases.
  Predict.
   
 

Question 19

Instructions: Predict the structure of the alkene you would use to prepare the folloiwng compounds. There may be more than one answer in some cases.
  Predict:
   
 

Question 20

What alkene would you use to prepare the following alkyl halide?
   
 

Question 21

The following reaction is carried out in cyclohexane with the application of heat. Write the complete equation for the reaction below. If more than one major organic product is expected, draw each one.
   
 

Question 22

Predict the major organic product(s) in the reaction below. If more than one major organic product is expected, draw each one. Explain the significance of 35C and ether shown in the reaction.
   
 

Question 23

Predict the major organic product(s) in the reaction below. If more than one major organic product is expected, draw each one.
   
 

Question 24

Alkene chemistry is dominated by what type of reaction?
  a.
  substitution
  b.
  electrophilic addition
  c.
  nucleophilic addition
  d.
  elimination
  e.
  both b and c

[aidanmbrowne]

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



Answer to Question 8



Answer to Question 9



Answer to Question 10

ANS: trans-1,2-dichlorocyclohexane

Answer to Question 11

c

Answer to Question 12



Answer to Question 13

Product B

Answer to Question 14

Product B

Answer to Question 15

b

Answer to Question 16



Answer to Question 17



Answer to Question 18



Answer to Question 19



Answer to Question 20

Only one alkene would be possible:



Answer to Question 21



Answer to Question 22


35C and ether are notes related to the reactions conditions. The reaction is carried out at 35C and the solvent is ether.

Answer to Question 23



Answer to Question 24

b

[Alainaaa8]

Gracias!

[TheNamesImani]

Great answer, keep it coming