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

Author Question: The heat of formation of 2-methylpropane is 32 kcal/mol. The heat of formation of butane is 30 ... (Read 101 times)

bcretired

  • Hero Member
  • *****
  • Posts: 525
The heat of formation of 2-methylpropane is 32 kcal/mol. The heat of formation of butane is 30 kcal/mol. The heat of hydrogenation of 2-methylpropene is 28 kcal/mol. What is the heat of formation of 2-methylpropene?
  1.4 kcal/mol
  2.2 kcal/mol
  3.2 kcal/mol
  4.4 kcal/mol
  5.60 kcal/mol

Question 2

How many degrees of unsaturation are there in the molecule of prizmane?
 
  1.1
  2.2
  3.3
  4.4
  5.5

Question 3

Which of the following bromides is the major product of the reaction shown below, assuming that there are no carbocation rearrangements?
 

Question 4

Which of the following -bonds participate in hyperconjugation?
 
  1.A and B
  2.A and E
  3.B and E
  4.C and D
  5.C and E

Question 5

Which statement best describes the energetics of the reaction shown below?
 
   C2H4 + H2  C2H6


  1.exothermic with positive activation energy
  2.exothermic with negative activation energy
  3.endothermic with positive activation energy
  4.endothermic with negative activation energy
  5.cannot be determined without knowing BDEs

Question 6

Which of the alkenes has the most negative heat of hydrogenation?
 

Question 7

What is(are) the double bond configuration(s) in the following compound?
 
  1. E
  2. Z
  3. E, Z
  4. E, E
  5. Z, Z

Question 8

Consider the reaction between HCl and ethene (the reactants). The carbocation intermediate and the Cl may revert to the reactants or go on to form the product, chloroethane. Which statement about this process is correct?
  1.The formation of chloroethane from the carbocation and Cl is the rate limiting process.
  2.The structure of the transition state for conversion of the carbocation to chloroethane resembles the product.
  3.The carbocation intermediate (and Cl) has energy that is intermediate between the reactants and the products.
  4.The intermediate may bond with Cl on either of its two carbons.
  5.Based on the Hammond postulate, the carbocation and Cl form the chloroethane faster than they revert to reactants.



Related Topics

Need homework help now?

Ask unlimited questions for free

Ask a Question
Marked as best answer by a Subject Expert

kiamars2010

  • Sr. Member
  • ****
  • Posts: 341
Answer to Question 1

4

Answer to Question 2

4

Answer to Question 3

5

Answer to Question 4

2

Answer to Question 5

1

Answer to Question 6

1

Answer to Question 7

4

Answer to Question 8

5




bcretired

  • Member
  • Posts: 525
Reply 2 on: Aug 23, 2018
Great answer, keep it coming :)


xiazhe

  • Member
  • Posts: 331
Reply 3 on: Yesterday
Wow, this really help

 

Did you know?

The types of cancer that alpha interferons are used to treat include hairy cell leukemia, melanoma, follicular non-Hodgkin's lymphoma, and AIDS-related Kaposi's sarcoma.

Did you know?

On average, the stomach produces 2 L of hydrochloric acid per day.

Did you know?

Nearly all drugs pass into human breast milk. How often a drug is taken influences the amount of drug that will pass into the milk. Medications taken 30 to 60 minutes before breastfeeding are likely to be at peak blood levels when the baby is nursing.

Did you know?

The lipid bilayer is made of phospholipids. They are arranged in a double layer because one of their ends is attracted to water while the other is repelled by water.

Did you know?

The Centers for Disease Control and Prevention (CDC) was originally known as the Communicable Disease Center, which was formed to fight malaria. It was originally headquartered in Atlanta, Georgia, since the Southern states faced the worst threat from malaria.

For a complete list of videos, visit our video library