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Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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
Transcribed Image Text:Which of the bases below would quantitatively deprotonate a terminal alkyne?
BuLi
B NH3
NaOH
D NaOCH2CH3
E t-BUOK
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- Indicate the product of Nucleophilic Substitution and Elimination of the following reactions(Note: draw proper settings when needed)arrow_forwardWhich statement best describes the first step in the mechanism of the following ether synthesis? Na + CH3I -OCH3 The alkoxide ion acts as a nucleophile and attacks the carbon of the alkyl halide. The alkoxide ion acts as a nucleophile and attacks the iodine of the alkyl halide. The alkoxide ion acts as an electrophile and attacks the iodine of the alkyl halide. The alkoxide ion acts as an electrophile and attacks the carbon of the alkyl halide.arrow_forwardIndicate, by letter(s), the position(s) on the ring at which substitution occurs when the aromatic compounds shown undergo bromination with Br₂, FeBr3 (when necessary). N(CH3)3 CN HN. C=O a b a O CH3 barrow_forward
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