1 circle the strongest nucleophile e d c b a h 2 o oh

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1. Circle the strongest nucleophile. E D C B A H 2 O OH - NH 2 - CH 3 CO 2 - NH 4 + 1. Circle the strongest nucleophile. (CH 3 ) 3 CO CH 3 O F CH 3 CO 2 CH 3 OH A B C D E 3. Circle the most stable carbocation. E D C B A CH 3 CHCH 3 CH 3 CH 2 CH 2 CH CH 2 4. Circle the most stable carbocation. E D C B A CH 3 CHCH 3 CH 2 CH CH 3 CH 2 5. Circle the alkyl halide that would react faster in a S N 1 reaction. Br Br CH 3 CH 2 CH 2 Br CH 3 C CH 2 Br A B C D CH 3 Br E 6. Circle the alkyl halide that would react faster in a S N 1 reaction. CH 3 CH 2 Br A B C D CH 3 Br E Ph 3 CBr CH 2 CHBr PhCH 2 Br 77. Circle the solvent that would make an S N 2 reaction go faster . E H 2 O CH 3 OH D C B A CH 3 CN CH 3 CH 2 CH 2 CH 2 CH 3 Cl 2 C CCl 2 8. Circle the alkyl halide that would react faster in a S N 2 reaction. CH 3 CH 2 Br A B C D CH 3 Br E (CH 3 ) 2 CHBr (CH 3 ) 3 CBr PhBr 3
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9. Which one of the following is a polar protic solvent? E CH 2 Cl 2 CH 3 OH D C B A CH 3 CN CH 3 (CH 2 ) 4 CH 3 CH 3 CH 2 OCH 2 CH 3 10. The most correct product(s) for the following reaction will be (HINT: is it S N 1 or S N 2?): 11. The predominant product produced in the following reaction is (Hint:
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