Using Ethylene, C₂H4, and methyl bromide, CH,Br, as your sole sources of carbon,propose a synthesis for -BuOH, (CH3),COH using the reactions that we covered thissemester in class up to now.*the synthesis should take about 7 steps and will include an alkylation and aGrignard reaction. Use one equivalent of methyl bromide for the alkylation step and usethe second one to make the Grignard reagent. The substrate in the Grignard reactionwill be a carbonyl - make this from your alkyne AFTER alkylation.*show all reactants and intermediates, and the reagents that you need for each step

To prepare tertiary butyl alcohol using ethylene and methyl bromide as the only sole sources of the carbon. The tertiary butyl alcohol can be synthesized from ethylene using the following set of reaction. (i) The first two steps involves in the synthesis of tertiary butyl alcohol (CH3)3COH is the conversion of ethylene to ethyne using Br2/CCl4 followed by the elimination reaction using the alc. KOH in the presence of heat. (ii) The next two steps involves the alkylation of alkyne formed which can be carried out by first treating the alkyne with a base like NaNH2 followed by the reaction with CH3Br. (iii) The next reaction involves the conversion of the prop-1-yne formed to acetone by Oxymercuration-demercuration reaction. (iv) The next step involves the formation of Grignard reagent by treating methyl bromide with magnesium in the presence of an ether. The final step involves the reaction of the Grignard reagent with acetone which results in the formation of tertiary Butyl alcohol.