3. Provide a complete synthesis for each of the following amines, no need for mechanisms CH3 1. AICI 3 2. H₂NNH2, KOH, A NMe NH2

Do both plz dont give incomplete solution DO BOTH MUST

E 21   write mechanisms for the given reactions

Presented 4 target molecules, A. Disconnect the target molecule so that a simple starting compoundcan be obtained B. Write down the possible synthesis reactions and the required reaction conditions Please Answer max in 30-40 minutes thank u so please

24-33 Predict the product(s) and provide the mechanism for each reaction below. denso od (a) 1. NaN3 2. H20, heat CI bns (b) REA 1. NaN3 on 2. H20, heat nl CI bauod di yd uo a done to m (c) COCI 1. NaN3 2. H20, heat H. (d) 1. NaN3 2. H20, heat CI

Nitration of methyl benzoate: Weight of filler paper: 0.682g Mp product: 76-77 C Nitration of Acetanilide: Weight of filler paper: 0.691g Weight of filler paper product: 1.232g Mp product: 212-214 C Compound MM (g/mol) ortho mp (oC) meta mp (oC) para mp (oC) Nitroacetanilide 180.16 94 155 214-217 Methyl nitrobenzoate 181.15 -13 78-80 94-96 Theoretical yield of acetanilde: 0.6664g  Theoretical yield of methyl benzoate: 0.7317g find theoretical yield of methyl nitrobenzoate                                              percent yield of your methyl nitrobenzoate and melting point of your methyl nitrobenzoate

propose a mechanism

What reaction sequence will form dibenylamine from benzoic acid in high yield

The enzyme hydroxynitrile lyase (HNL) catalyzes the conversion of cyanohydrins to HCN and a carbonyl compound, as shown below. OH HNL CN R' `R' HCN One of the proposed mechanisms for this enzyme is shown in the scheme below. His235 Ser80 Asp207. His235 0--H-N H Thr1 Asp207, O--H-N (a) Thr" Lys36O NH3 Lys2160 NH3 (d) N=C- OH HCN * H20 H20 His23 Sor80 His205 Asp207. Thr Asp207 Serão (b) O--H-N O The" IN=C Lys236O NH3 (c) NH5 (a) Describe the roles of Ser80, Lys 236, and His235 in catalysis.

Subject  :- Chemistry