5 What is the organic product? A. OH CH₂ (1) HgOAc₂ + H₂O (2) NaBH B. OH CH₂ C. он D. OH CH3

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
Question 5
6
Select one:
5 What is the organic product?
A.
OH
A. carbon ring.
B. C,C triple bond.
A.
OH
B.
(1) HgOAc₂ + H₂O
(2) NaBH₂
OH
C.
C,C double bond.
D. C,C single bond.
CH3
C.
?
он
D.
OH
The reaction of HCI with 1-pentene produces only one product,
2-chloropentane. Why does this product form instead of
1-chloropentane?
H+ and C know what the "EL-NM" rule is and dutifully
comply with it.
B. H+ bonds to the C-1 alkene carbon in the first step, forming
the more stable carbocation, with (+) charge on C-2,
followed by bonding of Cl nucleophile to positively charged
C-2.
C. There is less steric hindrance if Cl binds to C-2 and H+
bonds to C-1.
D. Cl bonds to the C-2 alkene carbon in the first step, forming
the more stable carbon anion with (-) charge on C-1,
followed by bonding of H* electrophile to (-) charged C-1.
Transcribed Image Text:6 Select one: 5 What is the organic product? A. OH A. carbon ring. B. C,C triple bond. A. OH B. (1) HgOAc₂ + H₂O (2) NaBH₂ OH C. C,C double bond. D. C,C single bond. CH3 C. ? он D. OH The reaction of HCI with 1-pentene produces only one product, 2-chloropentane. Why does this product form instead of 1-chloropentane? H+ and C know what the "EL-NM" rule is and dutifully comply with it. B. H+ bonds to the C-1 alkene carbon in the first step, forming the more stable carbocation, with (+) charge on C-2, followed by bonding of Cl nucleophile to positively charged C-2. C. There is less steric hindrance if Cl binds to C-2 and H+ bonds to C-1. D. Cl bonds to the C-2 alkene carbon in the first step, forming the more stable carbon anion with (-) charge on C-1, followed by bonding of H* electrophile to (-) charged C-1.
Expert Solution
steps

Step by step

Solved in 2 steps with 2 images

Blurred answer
Knowledge Booster
Carboxylic Acids and their Derivatives
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.
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