a.Which of the following compounds would you expect to react with a nucleophile atthe highest rate and why?NHF3CNHCF3NHCF3b. Reductions using LiAlH4 require a separate acid workup step, while reductionsusing NaBH4 do not.c. Aldehydes tend to be more hydrated that ketones.

The objective of the question is to find the following questions: Find the compound from the given…

a. Which of the following compounds would you expect to react with a nucleophile at the highest rate and why? ΝΗ NH I t F3C CF3 NH La CF3 b. Reductions using LiAlH4 require a separate acid workup step, while reductions using NaBH4 do not. c. Aldehydes tend to be more hydrated that ketones.

a. Which of the following compounds would you expect to react with a nucleophile at the highest rate and why? ΝΗ NH I t F3C CF3 NH La CF3 b. Reductions using LiAlH4 require a separate acid workup step, while reductions using NaBH4 do not. c. Aldehydes tend to be more hydrated that ketones.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Question

a.
Which of the following compounds would you expect to react with a nucleophile at
the highest rate and why?
NH
F3C
NH
CF3
NH
CF3
b. Reductions using LiAlH4 require a separate acid workup step, while reductions
using NaBH4 do not.
c. Aldehydes tend to be more hydrated that ketones.

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