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- please quickly thanks ! 3.Please write out the major reaction and side-reaction in the preparation of ter-butyl.chloride, and write out the key points to use separation funnel in this process.What is reaction 1 and 2 called? Choices: A. Williamson ether synthesis, B. Reduction with Grignard reagent, C. Acidic ether cleavage, D. FC Alkylation What are the reagents for reaction 1 and 2? Choices: A. methanol in acidic medium, B. sodium hydride and bromomethane, C. methyl bromide and aluminum bromide, D. methanoyl bromideI need specific description of the compounds involved in the synthesis (functional groups, specific features). and also describe the steps involved in the synthesis and the role of each step. And most important！！devote one to each step of the synthesis. Each step should clearly indicate the reagent used, the stereochemistry involved in the reaction and its importance or relevance to the multistep synthesis
- (a) Illustrate the following name reactions giving suitable example in each case :(i) Clemmensen reduction (ii) Hell-Volhard-Zelinsky reaction(b) How are the following conversions carried out?(i) Ethylcyanide to ethanoic acid (ii) Butan-l-ol to butanoic acid(iii) Benzoic acid to m-bromobenzoic acidcan i get help drawing out actual structures including the nucleophilic addition of Cy2NH to parafomaldehyde and its hemiaminal intermidiate and the condensation step when it is displaced by terminal alkyne forming allene, also what is dioxane getting rid of as the solvent, thanks(a) Illustrate the following name reactions giving a chemical equation in each case :(i) Clemmensen reaction (ii) Cannizzaro’s reaction(b) Describe how the following conversions can be brought about :(i) Cyclohexanol to cyclohexan-1-one (ii) Ethylbenzene to benzoic acid(iii) Bromobenzene to benzoic acid
- Choose the best reagents from the list provided below for carrying out the following conversion. Match the reagent with the step number. HCl (aq), Zn(Hg) KMnO4, H3O+ CH3Cl, AlCl3 HNO3, H2SO4 Cl2, FeCl3 fuming sulfuric acidPlease complete reactions in clear handwritten of all subpartsCH₂ + Using the reagents below, list in order (by letter, no period) those necessary to prepare 2-butyne from acetylene. Note: Not all spaces provided may be needed. Type "na" in any space where you have no reagent. a. Br₂, heat, light b. Na, (-H₂) c. Nal(SN2) d. NH4NO3 e. 1) NaNH2, liq. NH3, 2) CH3Br f. (CH3)3COK, (CH3)3COH, heat g. NaOEt, EtOH, heat Step #1 Step #2 Step #3
- Propose a short synthesis f or ONE of the following molecules. You can start with acetylene, and alkyl halides from 1-4 carbons in length. You can also use an reagents you wish. a) Hexan-3-one (CH3CH2COCH2CH2CH3)Give mekanisms for reaction 4a and 4 b. Question 5- show general mechanisms of carbonyl group(ketone, aldehyde) reacting in acidic conditions and basic conditions, explain the difference.Provide the reagent(s) for the reactions.