2) Draw the product of the following reaction: 1. BH, THE 2. HO, H₂O₂ 3. PCC 3) Which of the following statements is not true? A. Primary, secondary, and tertiary alcohols all undergo nucleophilic substitution with HI, HBr, and HCI. B. Carbocation stability: 1*> 2* > 3* C. Tertiary alcohols undergo SN1 reactions with hydrogen halides. D. Primary alcohols undergo SN2 reactions with hydrogen halides. E. An alcohol has a strongly basic leaving group that cannot be displaced by a nucleophile.

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
Question

I need help on #2 and #3 use image provided below 

1) When 1-pentanol is heated with HCI/ZnCl2, 1-chloropentane is the major product. This is an
is also produced as product.
reaction, and
A) SN1, H₂O
B) SN2, H₂O
C) SN1, H₂
D) SN2, H2
E) E2, H2
Chapter 10
2) Draw the product of the following reaction:
1. BH, THE
2 HỒ, HyOy
3. PCC
3) Which of the following statements is not true?
A. Primary, secondary, and tertiary alcohols all undergo nucleophilic substitution with HI,
HBr, and HCI.
B. Carbocation stability: 1*> 2* > 3*
C. Tertiary alcohols undergo SN1 reactions with hydrogen halides.
D. Primary alcohols undergo SN2 reactions with hydrogen halides.
E. An alcohol has a strongly basic leaving group that cannot be displaced by a nucleophile.
4) Using reagents such as SOCI₂ or PBrą, alcohols are converted into alkyl halides. This approach
A.
B.
C.
D.
E.
inverts the configuration if the OH group is bonded to an asymmetric center
converts the OH group into a better leaving group
works well for 1" and 2* alcohols
creates a leaving group that is a weaker base than the halide ion
does all of the above
Transcribed Image Text:1) When 1-pentanol is heated with HCI/ZnCl2, 1-chloropentane is the major product. This is an is also produced as product. reaction, and A) SN1, H₂O B) SN2, H₂O C) SN1, H₂ D) SN2, H2 E) E2, H2 Chapter 10 2) Draw the product of the following reaction: 1. BH, THE 2 HỒ, HyOy 3. PCC 3) Which of the following statements is not true? A. Primary, secondary, and tertiary alcohols all undergo nucleophilic substitution with HI, HBr, and HCI. B. Carbocation stability: 1*> 2* > 3* C. Tertiary alcohols undergo SN1 reactions with hydrogen halides. D. Primary alcohols undergo SN2 reactions with hydrogen halides. E. An alcohol has a strongly basic leaving group that cannot be displaced by a nucleophile. 4) Using reagents such as SOCI₂ or PBrą, alcohols are converted into alkyl halides. This approach A. B. C. D. E. inverts the configuration if the OH group is bonded to an asymmetric center converts the OH group into a better leaving group works well for 1" and 2* alcohols creates a leaving group that is a weaker base than the halide ion does all of the above
Expert Solution
steps

Step by step

Solved in 3 steps with 3 images

Blurred answer
Knowledge Booster
Alkynes
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
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