QUESTION 38 What kind of electrophile will you need to form the new bond identifed in Problem 35 and 36? O a. Sulfonate ester b. Aldehyde c. Carboxylic acid d. Alkyl halide (ex. XR) e. Ketone f. Ester O g. Epoxide
QUESTION 38 What kind of electrophile will you need to form the new bond identifed in Problem 35 and 36? O a. Sulfonate ester b. Aldehyde c. Carboxylic acid d. Alkyl halide (ex. XR) e. Ketone f. Ester O g. Epoxide
Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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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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Answer question 38 only!!
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![QUESTION 38
What kind of electrophile will you need to form the new bond identifed in Problem 35 and 36?
O a. Sulfonate ester
b. Aldehyde
O C. Carboxylic acid
d. Alkyl halide (ex. XR)
O e. Ketone
f. Ester
O g. Epoxide](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F3d365a50-fa77-4005-9109-a9cab1879229%2F0f57b111-ac02-4647-98e6-54c755c97147%2F9p3npl_processed.jpeg&w=3840&q=75)
Transcribed Image Text:QUESTION 38
What kind of electrophile will you need to form the new bond identifed in Problem 35 and 36?
O a. Sulfonate ester
b. Aldehyde
O C. Carboxylic acid
d. Alkyl halide (ex. XR)
O e. Ketone
f. Ester
O g. Epoxide
![QUESTION 35
For problems 35-40, answer the questions about the 2-step reaction sequence shown below.
OH
Reaction 3
Intermediate
Product Z
Br
Reaction 4
Number the carbons in your starting material. (This numbering scheme is arbitrary and is only intended to help you track where the carbons from your starting material appear in your product.) Identify those same carbons in your
final product and number them accordingly. What new type of bond has been formed?
O a. C=N
Ob.C-C
Occ-o
Od C-N
O e. C=C
Of. C=0
12:41 AM
QUESTION 36
Click on the location of the new bond you identified in the previous problem in the structure of the product shown below,
OH
Selected Coordinates
Clear
12:41 AM
QUESTION 37
What kind of nucleophile will you need to form the new bond identified in the previous two problems?
O a. Enolate
b. Tosylate
C. Alkoxide
d. Hydride reagent
e. Сyanide
O f. Organometallic reagent
O g. Pyridine
12:41 AM](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F3d365a50-fa77-4005-9109-a9cab1879229%2F0f57b111-ac02-4647-98e6-54c755c97147%2Flt1mpw_processed.jpeg&w=3840&q=75)
Transcribed Image Text:QUESTION 35
For problems 35-40, answer the questions about the 2-step reaction sequence shown below.
OH
Reaction 3
Intermediate
Product Z
Br
Reaction 4
Number the carbons in your starting material. (This numbering scheme is arbitrary and is only intended to help you track where the carbons from your starting material appear in your product.) Identify those same carbons in your
final product and number them accordingly. What new type of bond has been formed?
O a. C=N
Ob.C-C
Occ-o
Od C-N
O e. C=C
Of. C=0
12:41 AM
QUESTION 36
Click on the location of the new bond you identified in the previous problem in the structure of the product shown below,
OH
Selected Coordinates
Clear
12:41 AM
QUESTION 37
What kind of nucleophile will you need to form the new bond identified in the previous two problems?
O a. Enolate
b. Tosylate
C. Alkoxide
d. Hydride reagent
e. Сyanide
O f. Organometallic reagent
O g. Pyridine
12:41 AM
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