Chapter 7: PROBLEM 7.41 (page 290)
Question: Draw the products formed when each alkyl halide is treated with NaCN.
a.
b.
Chapter 7: PROBLEM 7.41 (page 290)
Question: Draw the products formed when each alkyl halide is treated with NaCN.
a.
b.
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Get started for freeQuestion: Explain why quinuclidine is a much more reactive nucleophile than triethylamine, even though both compounds have N atoms surrounded by three R groups.
Question: Identify the stronger nucleophile in each pair of anions.
a. Br- or Cl- in a polar protic solvent.
b. OH-or Cl- in a polar aprotic solvent.
c. HS- or F- in a polar protic solvent.
Question: Which solvents favor SN1reactions and which favor SN2 reactions?
a.
b. CH3CN
c.
d.
Question: Draw the product of nucleophilic substitution with each neutral nucleophile. When the initial substitution product can lose a proton to form a neutral product, draw the product after proton transfer.
a.
b.
Question: Draw the products of each SN1 reaction and indicate the stereochemistry of any stereogenic centers.
a.
b.
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