Rank the carbocations below in order of increasing stability ...

[karen]

Rank the carbocations below in order of increasing stability (least stable = 1; most stable = 3). Place the number corresponding to the carbocation's relative stability in the blank below the structure.
   
 

Question 2

Below are all the chemical structures and intermediates involved in a reaction. On the structures provided, show all electron flow using the arrow formalism for the complete stepwise mechanism.
   
 

Question 3

Predict the product of the following reaction of Prostaglandin H₂ by interpreting the flow of electrons as indicated by the curved arrows.
   
 

Question 4

The structures below show the stepwise bond making and bond breaking in this reaction. Draw curved arrows to show the electron flow that has occurred in each step.
   
 

Question 5

Instructions: Assign E or Z configurations to each alkene below.
  Assign:
   
 

Question 6

Instructions: Assign E or Z configurations to each alkene below.
  Assign:
   
 

Question 7

Which of the following substituents has the highest priority according to the Cahn-Ingold-Prelog system?
  a.
  -NH₂
  b.
  -NHCH₃
  c.
  -CH₂NH₂
  d.
  -CH₂NHCH₃

[gcook]

Answer to Question 1



Answer to Question 2



Answer to Question 3



Answer to Question 4



Answer to Question 5

e

Answer to Question 6

z

Answer to Question 7

b

[karen]

Great answer, keep it coming

[Dinolord]

Thanks for the timely response, appreciate it