2. CH3l Page< 4 > of 4 Q10. Apply retrosynthetic analysis to design a synthesis of the compound below, starting from an alkyne and an alkyl halide. DI 包 Q prtsc home end insert FB FIO F12
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- H. H ÔMe Ph;P LIAIH4 compound a compound b HO. Bombykol C16H300 The above reaction scheme presents one possible synthesis of the compound. Work out the synthesis on a separate sheet of paper, and then draw the structure of compound b. Consider E/Z stereochemistry of alkenes. Do not show stereochemistry in other cases.III. Propose a reasonable mechanism for the following reaction: & NaOH, H₂OWhat reagents are necessary to carry out the conversion shown? MgBr; Br Mg/ether; CrO3, H₂SO4; H 1. Mg/ether; 2. ; H3O+; PCC/CH₂Cl₂ H OLIAIH; H3O+; PCC/CH₂Cl2 ; H3O+; PCC/CH₂Cl2 H CI ; H3O+ ; 3. H3O+; 4. AICI 3
- OM on 2-mehoxybymethod.pentan 3omethylpentane,-2,B diudl Synthesize the ether product, 2-ethoxy-4-methyl pentane by two different methods out of various methods (nucleophilic substitutions, alkoxy mercuration/demercuration, industrial method (dehydration of alcohol), and Williamson method).Give detailed Solution with explanation needed...don't give Handwritten answerGive detailed mechanism Solution with explanation needed. Don't give Handwritten answer