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Q: Illustrate the Electrophilic Addition of H2O to an Alkene—Hydration ?
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A: The reaction is given below -
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- I recovered 3 mL of water, how many grams of water was produced in the reaction please show how? Cyclohexanol can attack the carbocation intermediate formed during the synthesis of cyclohexene. Draw this side product with the molecular formula C12H22O.Draw themajor product of this reaction. Ignore inorganic byproducts. PPC, CH2Cl2What is the product of the following reaction: Please don't provide handwriting solution
- A compound X with carbonyl groups was reduced using NaBH4 and the product is as shown in the photo. What is the possible structure of the starting compound?Draw the structure of the product of the reaction between the compound shown below and H2SO4.(please answer all questions) 1) Predict the products from reaction of 1-hexyne with thesereagents: a) One equivalent HBr b) One equivalent Cl2 c) H2 , Lindar Catalyst d) NaNH2 in NH3 , then CH3Br
- How combination of Br2 and H2O effectively forms bromohydrinsfrom alkenes ?Write an equation for the reaction of CH2=CHCH2CH3 with each of the following reagents: a. Ozone, followed by Zn, H+ b. BH3 followed by H2O2, OH c. Bromine Can you write it out please and thank youDraw the major product of this reaction. Ignore inorganic byproducts. 1. LiAIH4 2. Neutralizing work-up
- pls match them with the options, thats all What is the purpose of using the following chemicals in the preparation of n-butyl acetate? 1. Na2CO3 2. H2SO4 3. MgSO4 4. CH3COOH options: It is used as a dehydrating agent It is used as a catalyst It is used as a neutralizing substance for excess acid It is one of the reactantWhich of the following method is the best method for the synthesis of hexanal A.) Method: Ozonolysis, Reactant: Ozone, Substrate: 1-cyclopentyl-1-hexene B.) Method: Reduction, Reactant: LiAlH₄, Substrate: hexanoic acid C.) Method: Oxidation, Reactant: H₂CrO₄, Substrate: hexanol D.) Method: Oxidation, Reactant: KMnO₄, Substrate: hexanol E.) None of the given choicesAxial alcohols are oxidized faster than equatorial alcohols by PCC and other Cr6+ oxidants. Which OH group in each compound is oxidized faster?