each reagant must have 3 or less carbons . one image is the directions and one is the question. 11:50LTE 88zorXinorganicStarting from benzene synthesize ONE of the following compounds in good yield using aYou are welcome to use reactions wreagent or organic reagent with three or less carbons.didn't cover in lecture. YLanbinatar hu 11:50LTE 88synthesis. You should start with benzene and then addgroups. You can use any reagent if it is less than 3carbons unless it's just a reagent. For example, BuLi isokay, tosyl chloride is okay. You can use the Gilman or aGrignard if it is 3 or fewer carbons, but otherwise, youneed to make the carbon chain if it is more.X

The question is based on the concept of organic synthesis.We need to synthesize the product using reactants and reagents provided.In the first step, chlorination of benzene takes place to form chlorobenzene. It reacts with lithium and copper chloride to generate diphenyl cuprous lithium which is used during reaction synthesis.We start with benzene and carry out its nitration to form nitrobenzene. It undergoes friedel craft acylation reaction to introduce the Ketone group.Alpha bromination takes place to introduce bromine group followed by E2 elimination using potassium tert- butoxide to form less substituted alkene.Wolf Kischner reduction takes place to reduce ketone to corresponding hydrocarbon. anti markonikov addition of hydrogen bromide takes place across double bond to form less substituted bromide.It reacts with diphenyl cuprous lithium in a Corey house synthesis reaction to form C-C bond. nitro group gets reduced using tin and acid followed by diazotisation and reaction with hydrogen Tetrafluoro borate to introduce fluorine group.