56. Compound X (C;H12) is hydrogenated in the presence of Pd/BASO4 to produce (Z)-2-methyl- 3-hexene. What is the structure of X? the tansfor b. 2-methyl-3-hexyne low! a. 2-methyl-4-hexyne c. 2-methyl-4-hexene d. 2-methyl-4-hexane 57. How many meso compounds: CH3 CH Br Br CH3 CH b. 1 с. 2 d. 3 a. 0 58. Which of the following statements is (are) true for cis-1,2-dichlorocyclopropane? a. This compound is chiral. b. The enantiomer of this compound is trans-1,2-dichlorocyclopropane. c. This compound contains no asymmetric carbons. d. none of the above 59. Which structure provide (2R, 3S)-2-amino-3-hydroxybutanoic acid? он о он OH OH HO HO HO HO NH2 NH2 NH2 NH, D B
56. Compound X (C;H12) is hydrogenated in the presence of Pd/BASO4 to produce (Z)-2-methyl- 3-hexene. What is the structure of X? the tansfor b. 2-methyl-3-hexyne low! a. 2-methyl-4-hexyne c. 2-methyl-4-hexene d. 2-methyl-4-hexane 57. How many meso compounds: CH3 CH Br Br CH3 CH b. 1 с. 2 d. 3 a. 0 58. Which of the following statements is (are) true for cis-1,2-dichlorocyclopropane? a. This compound is chiral. b. The enantiomer of this compound is trans-1,2-dichlorocyclopropane. c. This compound contains no asymmetric carbons. d. none of the above 59. Which structure provide (2R, 3S)-2-amino-3-hydroxybutanoic acid? он о он OH OH HO HO HO HO NH2 NH2 NH2 NH, D B
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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![56. Compound X (C;H12) is hydrogenated in the presence of Pd/BASO4 to produce (Z)-2-methyl-
3-hexene. What is the structure of X?
ransforman
b. 2-methyl-3-hexyne
below
a. 2-methyl-4-hexyne
c. 2-methyl-4-hexene
d. 2-methyl-4-hexane
57. How many meso compounds:
CH3
CH3
Br Br
OH
CH,
CH3
a. 0
b. 1
с. 2
d. 3
58. Which of the following statements is (are) true for cis-1,2-dichlorocyclopropane?
a. This compound is chiral.
b. The enantiomer of this compound is trans-1,2-dichlorocyclopropane.
c. This compound contains no asymmetric carbons.
d. none of the above
then
59. Which structure provide (2R, 3S)-2-amino-3-hydroxybutanoic acid?
OH Oo
OH
OH
OH
HO
HO
HO
HO
NH,
NH,
NH2
NH2
B](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F684b437b-1c95-488b-8228-60dd67891e03%2F41e87a30-2e94-4112-9448-eba452ba6fb4%2Fl19f1lj_processed.jpeg&w=3840&q=75)
Transcribed Image Text:56. Compound X (C;H12) is hydrogenated in the presence of Pd/BASO4 to produce (Z)-2-methyl-
3-hexene. What is the structure of X?
ransforman
b. 2-methyl-3-hexyne
below
a. 2-methyl-4-hexyne
c. 2-methyl-4-hexene
d. 2-methyl-4-hexane
57. How many meso compounds:
CH3
CH3
Br Br
OH
CH,
CH3
a. 0
b. 1
с. 2
d. 3
58. Which of the following statements is (are) true for cis-1,2-dichlorocyclopropane?
a. This compound is chiral.
b. The enantiomer of this compound is trans-1,2-dichlorocyclopropane.
c. This compound contains no asymmetric carbons.
d. none of the above
then
59. Which structure provide (2R, 3S)-2-amino-3-hydroxybutanoic acid?
OH Oo
OH
OH
OH
HO
HO
HO
HO
NH,
NH,
NH2
NH2
B
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