Question

Please provide step 1 and 2

STANDARD VIEW PRINEER VERSION Practice Problem 21.82 Nitriles undergo alkylation at the a position much like ketones undergo alkylation at the a position BACK The a position of the nitrile is first deprotonated to give a resonance-stabilized anion (like an enolate), which then functions as a nucleophile to attack the alkyl halide. Dran the mechanism described above for the transformation below (propyl chloride will be the RX in this reaction). For the mechanism, draw the curved arrows as needed. Include lone pairs and charges in your answer. Do not draw out any hydrogen explicitly in your products. Do not use abbreviations such as Me or Ph. 1) LDA CN CN 2) RX Y Step 1 Get help answering Molecular Drawing questions. Incorrect. Which of the four mechanistic steps is shown in this step of the mechanism? Draw step 1 of the mechanism HE .CH. HE Edit CH. CH. LUNK 1O EX Attempts: 1 of 4 used SAVE FOR LAER SUBMIT ANswER Step 2 The parts of this question must be completed in order. This part will be available when you complete the part above

Answer 1

- ~ Step 1 EC:NO Step 11 of notre EN