QUE STION 35 For problems 35-40, answer the questions about the 2-step reaction sequence shown below. OH Reaction 3 Intermediate Product Z Reaction Br 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 O b. C-C Oc. C-O O d. C-N O e. C=c Or. C-O 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 QUESTION 37 What kind of nucleophile will you need to form the new bond identified in the previous two problems? O a. Enolate Ob. Tosylate OC. Alkoxide Od. Hydride reagent O e. Cyanide Of Organometallic reagent O 9. Pyridine

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Question #37 needed

QUESTION 35
For problems 35-40, answer the questions about the 2-step reaction sequence shown below.
OH
Reaction 3
Br
Intermediate
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?
О а. С-N
O b. C-C
О с. С-О
O d. C-N
O e. C=C
Of. C=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.
ОН
Selected Coordinates
Clear
QUESTION 37
What kind of nucleophile will you need to form the new bond identified in the previous two problems?
O a. Enolate
O b. Tosylate
O C. Alkoxide
O d. Hydride reagent
e. Cyanide
O f. Organometallic reagent
g. Pyridine
Transcribed Image Text:QUESTION 35 For problems 35-40, answer the questions about the 2-step reaction sequence shown below. OH Reaction 3 Br Intermediate 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? О а. С-N O b. C-C О с. С-О O d. C-N O e. C=C Of. C=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. ОН Selected Coordinates Clear QUESTION 37 What kind of nucleophile will you need to form the new bond identified in the previous two problems? O a. Enolate O b. Tosylate O C. Alkoxide O d. Hydride reagent e. Cyanide O f. Organometallic reagent g. Pyridine
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