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
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- QII: Starting from toluene as the only organic reagent you have and use any other inorganic reagents to prepare:What is the major organic product obtained from the following reaction? -- تمرة AICI 3 ب ب میں مجھ IV I OH3C 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
- Draw the skeletal structures of all the final organic products formed when phenol (C6H-OH) is treated with the set of reagents given below: OH HNO₂ H₂SO4 1) Sn, HC1 2) dilute aq NaOH ?H8.What is the major organic product of the following reaction? О O HO OH НО О нада О О НО + ОН ОН OH ногва H+ (cat.)
- Identify A, B, and C, intermediates in the synthesis of the five-membered ring called an α- methylene-γ-butyrolactone. This heterocyclic ring system is present in some antitumor agents.HelpDraw the structural formula of the enol formed in each alkyne hydration reaction; then draw the structural formula of the carbonyl compound with which each enol is in equilibrium