UP Academic League of Chemical Engineering Students (UP ALCHEMES)
UP Academic League of Chemical Engineering Students (UP ALCHEMES)
UP Academic League of Chemical Engineering Students (UP ALCHEMES)
A.
B.
C.
D.
D. 250
OH
A.
OH
6. Which is the most acidic?
B. CH3OH
C.
D. all of these
10. The methyl groups of cis-1,2-dimethylcyclohexane in the chair form will have a configuration of:
A. equatorial, equatorial
B. axial, equatorial
C. A & B
D. none of these
11. What alkene will yield CHO-CHO, CH2O, and OHCCH2CH3 upon ozonolysis followed by Zn, H2O,
H+?
A. CH2=CHCH2CH2CH=CH2
B. CH3CH=CHCH=CHCH3
C. CH2=CHCH=CHCH2CH3
D. CH2=CHCH=CHCH=CH2
12. What is the product formed when (CH3)2CHCH=CH2 undergoes acid-catalyzed hydration?
A. (CH3)2CHCH2CH2OH
B. CH3CH2CCH3OHCH3
C. (CH3)2CHCHOHCH3
D. all of these
13. What is the product formed when CH3CCH undergoes catalytic hydration?
A. CH3COCH3
B. CH3CHOHCH3
C. CH3CH2CH=O
D. CH3CH2CH3
14. How many mono-brominated products will 2,4-dimethylpentane give upon reaction with Br 2 under
UV light?
A. 1
B. 2
C. 3
D. 4
15. The pi electrons of an alkene act as the _____ in an electrophilic addition reaction.
A. electrophile
B. free radical
C. nucleophile
D. none of
these
16. Which of the following reactions of 2-butene will NOT follow Markovnikovs rule?
A. Reaction with H2O, H2SO4
B. Reaction with BH3, then with OH-, H2O2, H2O
C. Reaction with HCl
D. All will follow Markovnikovs rule
17. 2-butyne + _______ cis-2-butene
A. H2, Lindlars catalyst
B. H2, Pt
C. Na in liquid NH3 D. none of these
18. What is the product of the reaction of 1-methylcyclohexene and HBr?
A. 1-bromo-2-methylcyclohexane
B. 3-bromo-1-methylcyclohexene
C. 1-bromo-1-methylcyclohexane
D. 6-bromo-1-methylcyclohexene
19. Which of the following is a chain termination step?
A. A + B AB
B. A + B A + B C. A 2 A
D. none of these
B.
C.
23. In the more stable conformation of the cycloalkane below, the number of methyl groups in the
axial position is:
H3C
CH3
CH3
A. 3
B. 2
C. 1
D. 0
CH
CH3
24. Which of the following compounds would be the most stable free radical?
CH2
CH3
A.
CH3 H
H3C
H
CH3
B.
H3C
C.
CH3
25. The order of decreasing stability for the following
A
A. A>B>C
B
B. B>A>C
C. C>B>A
C
D. B>C>A
II. Draw at the back of this page what is described by each item.
1. The C5H12 isomer with the lowest boiling point.
2. The most stable C6H12 alkene.
3. The Haworth projection of cis-1,4-dimethylcyclohexane.
4. The most stable conformation of cis-1,4-dimethylcyclohexane.
5. Possible termination step in the free radical chlorination of CH 4.
III. Provide the missing starting material, reagents, intermediate, or product in each of the following
reactions.
B r2
h
(intermediate)
(Major product)
5
H 2O H
H 2O
N aO H , H 2O
B 2H
(intermediate)
(Major product)
H I
1) O
2 ) (C H 3)2S
8+9
21
C
C
H
22
CH
B 2H
H 2O
H
18
19 + 20
(intermediate)
(products)
15
H 2O
N aO H , H 2O
16
CH
ex cess H B r
17
14
1) O
2) Z n
N H
10
12
11
1) O
2 ) H 2O
13