Reviewquestions_19

Reviewquestions_19 - 1) Draw the structure of...

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1 1) Draw the structure of N -ethyl-N-methyl-1-hexanamine. Answer: Diff: 2
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2 8) Provide the systematic name for the compound below. Answer: 4-aminocyclohexanone Diff: 2 9) Provide the systematic name for the compound below. Answer: 2-bromo- N -methylaniline Diff: 2 21) Provide the product of the reaction shown below. Answer: Diff: 2 22) Circle the stronger base in the pair below, and briefly explain your choice. Answer: Pyrrolidine is the stronger base. Protonation of pyrrole results in loss of aromaticity. Diff: 3 23) Circle the stronger base in the pair below, and briefly explain your choice. Answer: Diethylamine is the stronger base. The lone pair electrons in pyridine are in an sp 2 orbital which is lower in energy than the sp 3 orbital of the lone pair in diethylamine. Diff: 3 24) Circle the stronger base in the pair below, and briefly explain your choice.
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Answer: Cyclohexylamine is the stronger base. The lone pair electrons in aniline are delocalized into the adjacent aromatic π system. Diff: 2
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This note was uploaded on 03/18/2010 for the course DSAG asdg taught by Professor Asdg during the Spring '10 term at 東京国際大学.

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Reviewquestions_19 - 1) Draw the structure of...

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