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Draw the structure of the major organic product(s) of the reaction.ClCH30. You do not have to consider stereochemistry.All carboxyl and amino groups should be drawn in the neutral form.If no reaction occurs, draw the organic starting material.Draw one structure per sketcher. Add addiional sketchers using the drop-down menu in the bottom right corner.Separate multiple products using the + sign from the drop-down menu.

Question

Draw the structure of the major organic product(s) of the reaction.

  • You do not have to consider stereochemistry.
  • All carboxyl and amino groups should be drawn in the neutral form.
  • If no reaction occurs, draw the organic starting material.
  • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
  • Separate multiple products using the + sign from the drop-down menu.
Draw the structure of the major organic product(s) of the reaction.
Cl
CH30
. You do not have to consider stereochemistry.
All carboxyl and amino groups should be drawn in the neutral form.
If no reaction occurs, draw the organic starting material.
Draw one structure per sketcher. Add addiional sketchers using the drop-down menu in the bottom right corner.
Separate multiple products using the + sign from the drop-down menu.
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Draw the structure of the major organic product(s) of the reaction. Cl CH30 . You do not have to consider stereochemistry. All carboxyl and amino groups should be drawn in the neutral form. If no reaction occurs, draw the organic starting material. Draw one structure per sketcher. Add addiional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu.

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Step 1

The reaction involves an acid chloride and an alcohol. An acid chloride reacts with an alcohol to form an ester. The ester is formed by losing a molecule of HCl from the acid chloride and the alcohol.

Step 2

The mechanism of the reaction is shown below. In the initial step of the reaction, the acid chloride undergoes nucleophilic attack by the alcohol with the loss of chloride ion. The complex then undergoes re-arrangement to form the desired ester.

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Step 3

The reaction is a simple SN2 type displacement reaction. The reaction proceeds easily without any c...

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Science

Chemistry

Carboxylic Acids

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