a. Draw the product of each of the following reactions: 1. NaH 1. CH3CH2C=CH 1. NaNH2 2. CH;CH,Br 2. CH;CH2CH,ОН 2. CH3Br b. Give two sets of reactants (each set including an alkyl halide and a nucleophile) that could be used to synthesize the following alkyne: CH;CH,C=CCH,CH,CH,CH3 c. Give two sets of reactants (each set including an alkyl halide and a nucleophile) that could be used to synthesize the following ether: CH;CH,OCH,CH,CHCH; CH3

Propose how you might synthesize the following molecules from an alkyl halide and a nucleophile.

Please help me find the SN1 product

Benzoyl chloride undergoes nucleophilic substitution at a faster rate than methyl propanoate because Select one: O a. the methoxide is a better leaving group than chloride. O b. chloride is a better leaving group than methoxide. O c. the acid chloride is more sterically hindered than the ester. O d. the ester is more sterically hindered than the acid chloride.

Which is the correct nucleophile in the following reaction? A. CH3MgBr 1) ? 2) H₂O OH B. CH3CH₂CH₂MgBr C. CH3CH₂MgBr D. PhMgBr

7. When the following ketone is treated with sodium hydroxide, two different enolates can form. a. Draw the two enolates, including an arrow pushing mechanism for their formation and any relevant resonance structures. NaOH b. Which enolate is favored when using sodium hydroxide as the base? Explain. c. Predict the product of the reaction and include an arrow-pushing mechanism. 1. NaOH 2. Br

1) The first mechanistic step of an acid catalyzed nucleophilic addition to a polar pi bond when the nucleophile is weak is which of the following? a. A nucleophile addition b. A proton transfer to the nucleophile c. A proton transfer from the nucleophile d. A proton transfer to the carbonyl e. A proton transfer from the carbonyl

What is the best choice of reagent(s) to perform the following transformation?

Draw the two starting materials that could be used to make the product via a Williamson ether synthesis.

1. Consider the two sets of reagents shown below. Set 1 Set 2 Br NaO ONa Br a. Which set of reagents will result in a successful Williamson Ether Synthesis? b. Starting from the successful set of reagents, draw the arrow-pushing mechanism leading to the ether product. What kind of reaction takes place (SN1, Sn2, E1, E2, acid/base)? Reaction Mechanism for successful reagent set Ether product c. What kind of reaction results from the other set of reagents? Draw the arrow-pushing mechanism for the major organic product that is formed. Reaction Mechanism for other reagent set Product