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- 3. Propose a plausible mechanism for the following transformation: & Q & CF3 H₂N CN 'N CF HOHPropose a plausible mechanism for the following transformation: 1) Excess MeMgBr 2) H₂O HOMustard gas, Cl¬CH2CH2¬S¬CH2CH2¬Cl, was used as a poisonous chemical agentin World War I. Mustard gas is much more toxic than a typical primary alkyl chloride. Itstoxicity stems from its ability to alkylate amino groups on important metabolic enzymes,rendering the enzymes inactive.(a) Propose a mechanism to explain why mustard gas is an exceptionally potent alkylatingagent
- Propose a detailed mechanism for the reaction below. HNO3 H₂SO4 NO₂Which reagent(s) would accomplish the synthesis showWn below? NH2 NH2 но. H3CO. A) NaBH4 В) РСС C) LAH D) Na2Cr207 / H2SO4 E) NAOH www w2) How would you synthesize the following compounds from cyclohexanone? CH₂Br CH₂C6H5 A Br B C D CH2CH2CO2H
- Provide a detailed arrow-pushing mechanism for the following transformation: Me PHOH PhO. Et Мe Me Et Me OTs Provide a detailed arrow-pushing mechanism for the following transformation:Draw the structure of all products of the mechanism below. H:I:SH 1:54 H₂N—C—C—C=c CH3 H H HTreatment of a cyclic ketone with diazomethane is a method for accomplishing a ring-expansion reaction. For example, treatment of cyclohexanone with diazomethane yields cycloheptanone. Propose a mechanism.
