ORGANIC CHEMISTRY

I. EASY
1. Which of the following compounds is the MOST reactive towards CH3CH2Cl, FeCl3 ? (10 Seconds)

A. B. C. D.

2. Which of the following is the MOST susceptible towards a nucleophile attack? (10 Seconds)

A. B. C. D.

3. Which of the following statements concerning the Friedel-Craft’s alkylation is correct? (15 Seconds)
I. The reactions is classified as an electrophilic aromatic substitution
II. Both aryl and alkyl halides may be used to initiate the reaction with the aromatic compound.
III. It involves the use of a Lewis Acid
IV. It involves the use of a Lewis Base

A. I and IV only B. I , II and IV C. I and III only D. I, II and III

4. For the given reaction below . Give the IUPAC Name of the major product. (15 Seconds)

5. For the given reaction below. Give the IUPAC Name of the major product . (15 Seconds)
II. AVERAGE
1. Given the following reaction. Draw the structure of the major product.(60 Seconds)

2. Given the following reaction. Give the IUPAC Name of the major product. ( 60 Seconds)

3. Given the following reaction . Give the IUPAC Name of the major product . ( 60 Seconds)

4. Give the IUPAC Name of the alkyl halide product for the following reaction. ( 60 Seconds)

5. Give the IUPAC Name of the major product for the following reaction. (45 Seconds)
III. DIFFICULT
1. Given the following reaction. Draw the structure of the major product. (120 Seconds)

2. Given the following reaction. Draw the structure of the major product. (120 Seconds)

3. Given the following reaction. Draw the structure of the major product. (150 Seconds)

4. Given the following reaction. Draw the structure of the final major product. (150 Seconds)
5. Give the IUPAC Name of the major product for the following reaction. (150 Seconds)
ANSWERS

I. EASY
1. C
2. A
3. C
4. Cyclohexa-1,4-diene or 1,4-Cyclohexadiene
5. Cyclopentanone

II. AVERAGE
1.

2. 2-Butanone
3. 2,3,4,5- Tetraiodopyrrole
4. 2-Bromo-2-Methylpropane
5. 3-Ethyl-5-Methylcyclohexanone

III. Difficult
1. 4.

2. 5. 3-Ethylpentane

3.