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 92 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
Wow, this really help


tranoy

  • Member
  • Posts: 344
Reply 3 on: Yesterday
Thanks for the timely response, appreciate it

 

Did you know?

Over time, chronic hepatitis B virus and hepatitis C virus infections can progress to advanced liver disease, liver failure, and hepatocellular carcinoma. Unlike other forms, more than 80% of hepatitis C infections become chronic and lead to liver disease. When combined with hepatitis B, hepatitis C now accounts for 75% percent of all cases of liver disease around the world. Liver failure caused by hepatitis C is now leading cause of liver transplants in the United States.

Did you know?

Acetaminophen (Tylenol) in overdose can seriously damage the liver. It should never be taken by people who use alcohol heavily; it can result in severe liver damage and even a condition requiring a liver transplant.

Did you know?

The most common treatment options for addiction include psychotherapy, support groups, and individual counseling.

Did you know?

The most common childhood diseases include croup, chickenpox, ear infections, flu, pneumonia, ringworm, respiratory syncytial virus, scabies, head lice, and asthma.

Did you know?

The training of an anesthesiologist typically requires four years of college, 4 years of medical school, 1 year of internship, and 3 years of residency.

For a complete list of videos, visit our video library