a) 1. Cl, 1-Pentene 2. NaNH,, heat b) 1. NaNH, Acetylene 2. CH,CH,CH,Br c) 1. NaNH,, NH, 1,1-Dichloropentane 2. H,0 d) All of these are effective 18 e) None of these are effective Question 37 Upon hydration of 2-heptyne in the presence of H9SO, and H2SO4, the two carbons of the triple bond are similarly but not identically substituted resulting in two regioisomeric enols, each of which gives a different ketone. Supply the names of the two enols formed. a) 2-heptanone and 3-heptanone b) 2-heptano and 3-heptanol c) 2-hepten-2-ol and hept-2-en-3-ol d) 3-hepten-3-ol and hept-3-en-4-ol e) 2-hepten-1-ol and 2-hepten-4-ol
a) 1. Cl, 1-Pentene 2. NaNH,, heat b) 1. NaNH, Acetylene 2. CH,CH,CH,Br c) 1. NaNH,, NH, 1,1-Dichloropentane 2. H,0 d) All of these are effective 18 e) None of these are effective Question 37 Upon hydration of 2-heptyne in the presence of H9SO, and H2SO4, the two carbons of the triple bond are similarly but not identically substituted resulting in two regioisomeric enols, each of which gives a different ketone. Supply the names of the two enols formed. a) 2-heptanone and 3-heptanone b) 2-heptano and 3-heptanol c) 2-hepten-2-ol and hept-2-en-3-ol d) 3-hepten-3-ol and hept-3-en-4-ol e) 2-hepten-1-ol and 2-hepten-4-ol
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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![Question 36
Which of the following is an effective way to prepare 1-pentyne?
a)
1. Cl,
1-Pentene
2. NaNH,, heat
b)
1. NaNH,
Acetylene
2. CH,CH,CH,Br
c)
1. NANH,, NH,
1,1-Dichloropentane
2. H,0
d) All of these are effective
18
e) None of these are effective
Question 37
Upon hydration of 2-heptyne in the presence of HgSO, and H2SO4, the two
carbons of the triple bond are similarly but not identically substituted resulting in
two regioisomeric enols, each of which gives a different ketone. Supply the
names of the two enols formed.
a) 2-heptanone and 3-heptanone
b) 2-heptano and 3-heptanol
c) 2-hepten-2-ol and hept-2-en-3-ol
d) 3-hepten-3-ol and hept-3-en-4-ol
e) 2-hepten-1-ol and 2-hepten-4-ol](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F80beb3c7-0805-4123-826a-93aa0f72cc1c%2F2c201d21-edae-4c2a-ba5c-7a58513d9119%2F7qfhw3_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Question 36
Which of the following is an effective way to prepare 1-pentyne?
a)
1. Cl,
1-Pentene
2. NaNH,, heat
b)
1. NaNH,
Acetylene
2. CH,CH,CH,Br
c)
1. NANH,, NH,
1,1-Dichloropentane
2. H,0
d) All of these are effective
18
e) None of these are effective
Question 37
Upon hydration of 2-heptyne in the presence of HgSO, and H2SO4, the two
carbons of the triple bond are similarly but not identically substituted resulting in
two regioisomeric enols, each of which gives a different ketone. Supply the
names of the two enols formed.
a) 2-heptanone and 3-heptanone
b) 2-heptano and 3-heptanol
c) 2-hepten-2-ol and hept-2-en-3-ol
d) 3-hepten-3-ol and hept-3-en-4-ol
e) 2-hepten-1-ol and 2-hepten-4-ol
![Question 35
Upon carrying out mechanisms for each of the following reactions, which of the
following reactions will not yield a secondary alcohol?
a)
H,SO,/H,0
b)
1) Hg(OAc),/H,0
2) NaBH,/OH
c)
1) ВН, THF
2) H,O,/OH
d)
17
1) Hg(OAc)/H,0
2) NABH,/OH
e) none of the above](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F80beb3c7-0805-4123-826a-93aa0f72cc1c%2F2c201d21-edae-4c2a-ba5c-7a58513d9119%2F271dh4h_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Question 35
Upon carrying out mechanisms for each of the following reactions, which of the
following reactions will not yield a secondary alcohol?
a)
H,SO,/H,0
b)
1) Hg(OAc),/H,0
2) NaBH,/OH
c)
1) ВН, THF
2) H,O,/OH
d)
17
1) Hg(OAc)/H,0
2) NABH,/OH
e) none of the above
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