EBK ESSENTIAL ORGANIC CHEMISTRY
EBK ESSENTIAL ORGANIC CHEMISTRY
3rd Edition
ISBN: 8220100659461
Author: Bruice
Publisher: PEARSON
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Chapter 13, Problem 27P

Explain why the pKa of a hydrogen bonded to the sp3 carbon of propene is greater (pKa = 42) than that of any of the carbon acids listed in Table 13.1, but is less than the pKa of an alkane (pKa > 60).

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2. Draw structures for the following systems. If more than one isomer is possible, draw strcutures for all the possible isomers. Benzene ring with a methyl group and a nitro group (Draw all possible isomers, and name them) Benzene ring connected to a heptane chain (Draw all possible isomers, and name them) 2-benzyl-3- methylbutan-1-ol
What accounts for the geometry (pyramidalization) of the NH2 group in aniline? 1. Resonance between the NH2 group and the benzene ring. 2. The electronic withdrawing nature of the sp2 carbons in the phenyl group. 3. Participation of the nitrogen lone pair to make the system aromatic. 4. Both 1 and 3.
True or False 1. With alkynes having 2 pi bonds, they have more electron-rich region than alkenes and, thus, are more reactive than alkenes. 2. Hydrobromination of an alkene follows anti-Markovnikov’s rule in the presence of a peroxide. 3. The reaction of BH3 with 2-methylbut-2-ene results in the attachment of a hydroxyl group, OH, on the third carbon since this carbon is less substituted. 4. The reduction of an alkyne using a strong base such as LiNH2 gives an alkane when 2 equivalents of hydrogen gas is added.
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