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- The reaction of 2-ethyl-1-pentene with Br2, with H2 + Pd/C, or with R2BH/THF followed by aqueous HO- + H2O2 leads to a racemic mixture. Explain why a racemic mixture is obtained in each case.Predict the product of the following reaction and classify the reaction Pb+FeSO4---> PbSO4+ ______predict the products: XCL2+ E3PO4 --->
- Write the products of the reaction below and indicate if the product is R or S or racemic or achiral.Predict the major products of the following reactions, including stereochemistry.(a) cyclohexene + KMnO4>H2O (cold, dilute)List the following in increasing order of nucleophilic strength. CH3COO-, H2O, CH3O-, OH-, CH3CH20-
- What is the major product obtained from treating an excess of each of the following compounds with Cl2 in the presence of ultraviolet light at roomtemperature? Disregard stereoisomers.1-Bromobutane would react with HS- via _______ reactiona.) SN1 b.) SN2 c.) E1 d.) E2Predict the major products of the following reactions. Include stereochemistry whereapplicable.(a) 1@methylcycloheptene + BH3 # THF, then H2O2, OH
- What is the major product obtained from treating an excess of each of the following compounds with Cl2 in the presence of ultraviolet light at room temperature? Disregard stereoisomers.The reaction of (S)-2-bromopentane with potassium cyanide to yield 2-methylpentanenitrile (2-cyanopentane) occurs due to a nucleophilic substitution pathway. The reaction is 100% stereospecific. Please explain what this observation tells about the mechanism of the reaction.Which of the following is/are the expected product/s of the reaction of 2-pentanone (CH3COCH2CH2CH3) with excess Br2, followed by OH-? CHBr3 + CH3CH2CH2COOH BrCH2COCH2CH2CH3 CHBr3 + CH3CH2CH2COO- CH3COCHBrCH2CH3