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 ca final product and number them accordingly What new type of bond has been formed? O a. C=N Ob.C-C Ос со OdCN O e. C=C Of. C=0

Organic Chemistry
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Chapter9: Alkynes: An Introduction To Organic Synthesis
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Problem 46AP: A hydrocarbon of unknown structure has the formula C8H10. On catalytic hydrogenation over the...
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QUESTION 35
For problems 35-40, answer the questions about the 2-step reaction sequence shown below
OH
Reaction 3
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?
O a. C=N
Ob.c-C
Oc co
Od C-N
O e.C=c
Of. C=0
12:41 Aivi
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?
a. Enolate
b. Tosylate
O C. Alkoxide
O d. Hydride reagent
e. Сyanide
O f. Organometallic reagent
O g. Pyridine
12:41 AM
QUESTION 38
What kind of electrophile will you need to form the new bond identifed in Problem 35 and 36?
a. Sulfonate ester
b. Aldehyde
c. Carboxylic acid
d. Alkyl halide (ex. XR)
e. Ketone
f. Ester
O g. Epoxide
12:41 AM
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 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 Oc co Od C-N O e.C=c Of. C=0 12:41 Aivi 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? a. Enolate b. Tosylate O C. Alkoxide O d. Hydride reagent e. Сyanide O f. Organometallic reagent O g. Pyridine 12:41 AM QUESTION 38 What kind of electrophile will you need to form the new bond identifed in Problem 35 and 36? a. Sulfonate ester b. Aldehyde c. Carboxylic acid d. Alkyl halide (ex. XR) e. Ketone f. Ester O g. Epoxide 12:41 AM
QUESTION 39
Is Intermediate Z the nucleophile or the electrophile?
O Neither!
O Electrophile!
O Nucleophile!
Transcribed Image Text:QUESTION 39 Is Intermediate Z the nucleophile or the electrophile? O Neither! O Electrophile! O Nucleophile!
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