3 of 8 Level 2 1a. Draw in the arrow-pushing for the reaction below, which makes a precursor for the cyanosulfidic synthesis. Label the nucleophile and electrophile in the boxed step, and what is X? © NH4 HN OH © NH NH3 L H₂NO OH HN OH NH2 HO HO NH₁₂ HN © NH4 H₂N HO HO NH3 -X NH4 H₂N 1b. The first step of the reaction is inhibited by excess cyanide anion. What does the cyanide react with (the glycolaldehyde or the aminonitrile)?

3 of 8 Level 2 1a. Draw in the arrow-pushing for the reaction below, which makes a precursor for the cyanosulfidic synthesis. Label the nucleophile and electrophile in the boxed step, and what is X? © NH4 HN OH © NH NH3 L H₂NO OH HN OH NH2 HO HO NH₁₂ HN © NH4 H₂N HO HO NH3 -X NH4 H₂N 1b. The first step of the reaction is inhibited by excess cyanide anion. What does the cyanide react with (the glycolaldehyde or the aminonitrile)?

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.SE: Something Extra

Problem 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...

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