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- Draw the organic products formed when allylic alcohol A is treated with each reagent.a.H2 + Pd-C b.mCPBA c. PCC d.CrO3, H2SO4, H2O e.(CH3)3COOH, Ti[OCH(CH3)2]4, (+)-DET f. (CH3)3COOH, Ti[OCH(CH3)2]4, (−)-DET g. [1] PBr3; [2] LiAlH4; [3] H2O h.HCrO4−–Amberlyst A-26 resinDraw the products formed when p-methylaniline (p-CH3C6H4NH2) istreated with following reagent. Part (b), then CH3COCl, AlCl33-pentanol reaction to HOCl
- Starting with cyclohexanone, show how to prepare these compounds. In addition to the given starting material, use any other organic or inorganic reagents as necessary. Q.) cis-1,2-CyclohexanediolWhat product is obtained from the reaction of excess benzene with 1-chloro-2,2-dimethylpropane + AlCl3 ?cis-Cyclohexane-1,2-diol can be synthesized from cyclohexene by using which reagent? a.O3 b.OsO4 c.H2SO4 d.mCPBA
- In addition to using CHX3 and base to synthesize dihalocarbenes (Section 26.4), dichlorocarbene (:CCl2) can be prepared by heating sodium trichloroacetate. Draw a stepwise mechanism for this reaction.#20 B Draw structural formulas for all possible carbocations formed by the reaction of each alkene with HCl.the reagents are LiAlH4 Et2O / H2O, can you please redo with these reagents? Thank you.
- Draw a stepwise mechanism for the sulfonation of an alkyl benzene such as A to form a substituted benzenesulfonic acid B. Treatment of B with base forms a sodium salt C that can be used as a synthetic detergent to clean away dirt (see Problem 3.22).Starting with cyclohexanone, show how to prepare these compounds. In addition to the given starting material, use any other organic or inorganic reagents as necessary. Q.) CyclohexeneDraw the organic products formed when attached allylic alcohol A is treated with following reagent. (CH3)3COOH, Ti[OCH(CH3)2]4, (+)-DET