33. What reagents in the order written below would accomplish the following transformation? CI A) 1) Mg in ether; 2) B) 1) HCC?; 2) HgSO4, C) 1) Mg in ether; 2) 0 H; 3) H₂O H₂SO4, H₂O; 3) NaBH4, CH₂OH ; 3) H₂O THE: 3) H₂O2, NaOH

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...
icon
Related questions
icon
Concept explainers
Question

Organic Chemistry, see image for questions 

 

33. What reagents in the order written below would accomplish the following transformation?
A) 1) Mg in ether; 2)
"H; 3) H₂O
B) 1) HCC?; 2) HgSO4, H₂SO4, H₂O; 3) NaBH4, CH₂OH
A
C) 1) Mg in ether; 2)
; 3) H₂O
D) 1) HCEC?; 2) 9-BBN, THF; 3) H₂O2, NaOH
34. What is the final product obtained from the following transformation sequence: 1-pentyne
reacted with 1) NaNH2, 2) ethyl iodide, 4) H2, Pd, BaSO4, quinoline, MeOH 5) Br2 ?
A. 1&2
1
Br
Br
B. 1&3
Br
B
2
Br
C. 2&3
3
C
Br
Br
D. 3&4
35. Choose the molecule that will favor 1,2-methide shift readily upon hydration reaction under
acidic conditions?
Br
D
4
Br
D. 75%
calculate the percent enantiomeric excess of S stereoisomer in a mixture that contains 75
cent S stereoisomer and 25 percent R stereoisomer
-0%
B. 60%
C. 70%
Transcribed Image Text:33. What reagents in the order written below would accomplish the following transformation? A) 1) Mg in ether; 2) "H; 3) H₂O B) 1) HCC?; 2) HgSO4, H₂SO4, H₂O; 3) NaBH4, CH₂OH A C) 1) Mg in ether; 2) ; 3) H₂O D) 1) HCEC?; 2) 9-BBN, THF; 3) H₂O2, NaOH 34. What is the final product obtained from the following transformation sequence: 1-pentyne reacted with 1) NaNH2, 2) ethyl iodide, 4) H2, Pd, BaSO4, quinoline, MeOH 5) Br2 ? A. 1&2 1 Br Br B. 1&3 Br B 2 Br C. 2&3 3 C Br Br D. 3&4 35. Choose the molecule that will favor 1,2-methide shift readily upon hydration reaction under acidic conditions? Br D 4 Br D. 75% calculate the percent enantiomeric excess of S stereoisomer in a mixture that contains 75 cent S stereoisomer and 25 percent R stereoisomer -0% B. 60% C. 70%
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 3 steps with 2 images

Blurred answer
Knowledge Booster
IR Spectroscopy of Organic Molecules
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Chemistry
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY