Draw the structures of all the products that can be formed by the reaction of p-bromotoluene with sodium amide in ammonia at -33 °C. Br NINH, NH, '2' -33°C 3

Write the corresponding products or reagents where necessary to obtain the products.

What is the major organic product obtained from the following reaction? -- تمرة AICI 3 ب ب میں مجھ IV I O

H3C OH OH H+ CH3 Esters can be synthesized by an acid-catalyzed nucleophilic acyl substitution between an alcohol and a carboxylic acid; this process is called the Fischer esterification reaction. Because the alcohol oxygen is a poor nucleophile, the carbonyl carbon is made a better electrophile by protonation of the carbonyl oxygen. The steps of the synthesis are all reversible. The reaction is generally driven to completion by using an excess of the liquid alcohol as a solvent, or by distilling off the product as it forms. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions CIX 10-4 H₂O CH3 H₂O CH3