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- Do not give handwriting solution. please draw out what compound A is and then provide aroow pushing mechanism for thisreaction! thanks01 Cive the ctrientiono of Comnand 4 2.2 Provide a reasonable arrowpushing mechanism for the reaction in 2.1Nitrating methyl benzoate. 1.Describe the mechanism of EAS clearly and in detail 2. What is the effect of subtituent of the outcome of EAS;include 3 classes of subtituentsPropose a mechanism for the followingreaction.
- Please draw the mechanism (assuming an SN1pathway) for the reaction of cyclopentyl bromide with the cyanide anion (-CN) to yield cyclopentyl cyanide as the organic product Thank you-Reactions E1 and E2 with AlcoholsIt develops the following reaction mechanisms and the main and secondary products:Give the major organic product of the following reaction sequences (d & e).
- For butenafine, develop a synthesis that starts with napthalene and benzene. (aromatic methyl groups can be converted to alkyl bromides using Br2/light, and aldehydes by heating the alkyl bromide in DMSO, eg. ArCH3 to ArCH2Br then to ArCHO).Please give the mechanism of all the reaction. Thanks in advance!Give a clear explanation of how the followingcarbocation is stabilized:
- Propose a plausible mechanism for the following formation:a,b-Unsaturated carbonyl compounds are susceptible to either 1,2 addition or 1,4 (Michael)addition. Give examples of nucleophiles that would favor each case and explain yourreasoningWhich compound is not a possible product in the reaction below ( F2 is in excess F2and UV light the catalyst).CHA + F2 -->O CFAO CHFaO CHF-O CH2F2O CHaF