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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 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
Chemistry
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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
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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
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
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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