1. Show how to bring about each step in this synthesis of the herbicide propranil. NHCCH.CH...
2. Show how to bring about each step in the following synthesis of N-methyl-o-toluidine. WCH ACH ACH, ACHACH, ( NO, NH, VCN CHANH,
How wond you carry out the synthesis below? Show the reagents needed for each step of your transformation, but do not draw the mechanisms for each step. NH2 ---> N
Using the reagents listed in the table below, show how to bring about the following conversion: (Specify the reagents you would use to carry out the conversion by using letters from the table. A step may require more than one reagent, if so, write the letters in the order that they are used, e.g., if. If two or more ways of conversion to the same product are possible, show only one of them.) The reagents are (in order of use)...
Draw the structure of the product of each step in the following three- step synthesis. Show all formal charges.
Draw the structure of the product of each step in the following three-step synthesis. Show all formal charges.
20% Multi-Step Synthesis Sa) Show how you could perform the following synthesis. You may use any reagents that you need.
20% Multi-Step Synthesis Sa) Show how you could perform the following synthesis. You may use any reagents that you need.
Draw the structure of the major product of each step in the
following three-step synthesis. Show the formal charges, where
applicable. As a start, the benzene ring is drawn for you in each
product.
Draw the structure of the product of each step in the following
three-step synthesis. Show the formal charges, if applicable. As a
start, the benzene ring is drawn for you in each product. Although
the first step produces a mixture of isomers, the para isomer is
isolated as the sole product of interest and used in the second
step. Give only the major product for the second and third
steps.
Draw the structure of the product of each step in the following
three-step synthesis. Show the formal charges, if applicable. As a
start, the benzene ring is drawn for you in each product. Although
the first step produces a mixture of isomers, the para isomer is
isolated as the sole product of interest and used in the second
step. Give only the major product for the second and third
steps.
show how you would bring about this conversion
(m) propene to acetone