Chapter L3, Problem 9E

Predict the product of the following reaction. 1st attempt HI 1 product 50300 Jul See Periodic Table See Hint P Br 石尚 I

Indicate the substitutes in one place, if they are a diazonio room.

Indicate the product formed in each reaction. If the product exhibits tautomerism, draw the tautomeric structure. a) о + CH3-NH-NH2 CO2C2H5 b) + CoH5-NH-NH2 OC2H5

Indicate the formula of the compound, that is the result of the N- alquilación (nucleofílic substitution), in which an additional lateral chain was formed (NH-CH2-COOMe). F3C. CF3 NH NH2 Br о OMe K2CO3, DABCO, DMF

Synthesis of 1-metilbenzotriazole from 1,2-diaminobenceno.

Synthesis of 1-metilbenzotriazole.

Indicate the formula of the compound, that is the result of the N- alquilación (nucleofílic substitution), in which an additional lateral chain was formed (NH-CH2-COOMe). F3C. CF3 NH NH2 Br о OMe K2CO3, DABCO, DMF

Identify the mechanism through which the following reaction will proceed and draw the major product. Part 1 of 2 Br KOH EtOH Through which mechanism will the reaction proceed? Select the single best answer. E1 E2 neither Part: 1/2 Part 2 of 2 Draw the major product formed as a result of the reaction. Click and drag to start drawing a structure. X

What is single-point calibration? Provide an example.