Chapter 17: 17-56P (page 847)
What is the product of the following reaction?
Chapter 17: 17-56P (page 847)
What is the product of the following reaction?
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Get started for freeQuestion: Explain why the -hydrogen of an N,N-disubstituted amide is less acidic (pKa= 30) than the hydrogen of an ester (pKa= 25).
Propose a mechanism for the following reaction:
Explain why the pKaof a hydrogen bonded to the sp3carbon of propene is greater (pKa= 42) than that of any of the carbon acids listed in Table 17.1, but is less than the pKaof an alkane (pKa> 60).
When a dilute solution of acetaldehyde in D2O containing NaOD is shaken, explain why the methyl hydrogens are exchanged with deuterium but the hydrogen attached to the carbonyl carbon is not.
How could you prepare the following compound using a starting material that contains no more than three carbons?
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