QUESTION 35 For problems 35-40, answer the questions about the 2-step reaction sequence shown below. Reaction Intermediate Product Z Reaction 4 Number the carbons in your starting malerial. (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 bong has been fomed? Oa C-N Od.CN Oe C-C OL CrO QUE STION 36 Click on the location of the new bond vou identified in the previous problem in the structure of the product shown below, OH Selected Coordinates Clear QUE STION 37 What kind of nucleophile wil you need to form the new bond identified in the previous two problems? Oa Enolate Ob Tosylate OC Alkaxide Od Hydride reagent Oe Cyanide OL Organometallc reagent yridine QUE STION 38 What kind of electrophle will you need to form the new bond identifed in Problem 35 and 36? Oa Sulfonate ester Ob. Aldehyde Oc Carbaxylic acid Od. Alky halide (ex. XR) Oe Ketone OL Ester g. Epoxide
QUESTION 35 For problems 35-40, answer the questions about the 2-step reaction sequence shown below. Reaction Intermediate Product Z Reaction 4 Number the carbons in your starting malerial. (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 bong has been fomed? Oa C-N Od.CN Oe C-C OL CrO QUE STION 36 Click on the location of the new bond vou identified in the previous problem in the structure of the product shown below, OH Selected Coordinates Clear QUE STION 37 What kind of nucleophile wil you need to form the new bond identified in the previous two problems? Oa Enolate Ob Tosylate OC Alkaxide Od Hydride reagent Oe Cyanide OL Organometallc reagent yridine QUE STION 38 What kind of electrophle will you need to form the new bond identifed in Problem 35 and 36? Oa Sulfonate ester Ob. Aldehyde Oc Carbaxylic acid Od. Alky halide (ex. XR) Oe Ketone OL Ester g. Epoxide
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 #38 needed
![QUESTION 35
For problems 35-40, answer the questions about the 2 slep reaction sequence shown below.
HO
Reaction 3
Br
Intermediale
Product Z
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 C-N
O e C=C
OLC-0
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
QUE STION 37
Whal kind of nucleophlle will you need to form the new bond identified in the previous two problems?
O a. Enolate
Ob. Tosylate
O C. Alkoxide
O d. Hydride reagent
O e. Cyanide
Of. Organometallic reagen!
9 Pyridine
QUE STION 38
What kind of electrophille will you need to form the new bond identifed in Problem 35 and 36?
O a. Sulfonate ester
O b. Aldehyde
O Carboxylic acid
Od. Alkyl halide (ex. XR)
O e. Ketone
OL Ester
O9 Epoxide](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fe45c1097-c18b-4e35-a91b-ef162f0e41af%2Fb4e802ca-2472-483a-b046-fba2ad5c83c1%2F93svwa9_processed.jpeg&w=3840&q=75)
Transcribed Image Text:QUESTION 35
For problems 35-40, answer the questions about the 2 slep reaction sequence shown below.
HO
Reaction 3
Br
Intermediale
Product Z
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 C-N
O e C=C
OLC-0
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
QUE STION 37
Whal kind of nucleophlle will you need to form the new bond identified in the previous two problems?
O a. Enolate
Ob. Tosylate
O C. Alkoxide
O d. Hydride reagent
O e. Cyanide
Of. Organometallic reagen!
9 Pyridine
QUE STION 38
What kind of electrophille will you need to form the new bond identifed in Problem 35 and 36?
O a. Sulfonate ester
O b. Aldehyde
O Carboxylic acid
Od. Alkyl halide (ex. XR)
O e. Ketone
OL Ester
O9 Epoxide
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