Chapter 18, Problem 35P

E!!- Alkyl halide: Same as SNI Bay / NU! Same as SN' in presence of heat -OH H₂say

Name four ways to increase the rate of a reaction.

HO (c) (1 pt) Both of the following are hydride donors. Circle the harder nucleophile of -P-Cu-H H + H-AI-H H (d) (4 pts) The following reaction involves two steps. Draw the anionic intermediate that forms after sodium hydride reacts and the final organic product. Hints: what type of nucleophile is NaH and where does that mean it will react? Also, the second step is not a proton transfer. What's the most likely reaction for that intermediate to undergo? NaH anionic intermediate final product