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- r Plase don't provide handwritten solution Write carbonyl compound & phosphonium ylide that yield below alkene upon reactionShow how m-dibromobenzene can be synthesized from benzene from multiple reactions. Tip: think of diazotation as an important reaction in this process.(A) Provide the major organic product for the reaction below (B) Would the product be optically active of optically in active?
- Please help with the following ochem mechanisms.... 1. Provide the stepwise mechanisms for the following reactions (see attached picture)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 2.1Please 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
- Answer all questions. ai. Give the structure of the product formed from the reaction of propanal with 1M ethanol in dry acid. ii. What happens when Further 1M of ethanol is added to the reaction in i above?give clear handwritten answer please-Given tautomerization mechanism thatcontains multiple errors. Selectany errors that occur in step 1 ofthe mechanism-(please give clear handwritten answer) Draw the structure of compound P and discuss the mechanism of the reaction of compounds N and O to give compound P, Figure 8. What is the name of this reaction?
- A. Provide the necessary reagents. B. Provide the necessary eragnets and the step by step mechanism.Draw the ALL of the E2 organic product formed when the structure shown below undergoes dehydrohalogenation in KOH with heat.Please provide the answers in each situation. 1. Which compound/s will react with Br2 in water under light conditions? (answer may be one or more) 2. Which compund/s will react with I2 in KI under dark conditions? (answers may be one or more)