Which class of addition reaction is represented by the transformation below: + Br OH O dihydroxylation ○ hydration O halohydrin formation ○ hydrogenation ozonolysis hydrohalogenation O halogenation
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- Draw structures of compounds that fit the following descriptions: a) An , unsaturated ketone, C9H8O b) An diketone c) An aromatic ketone, C9H10O d) A diene aldehyde, C7H8OWhat is the type of following reaction? O Elimination Rearrangement Substitution Addition + Cl₂ — Cl ∞ Cl + HC1Which class of addition reaction is represented by the transformation below: O dihydroxylation O hydration halogenation halohydrin formation O hydrogenation hydrohalogenation O ozonolysis OH OH
- When propene reacts with gaseous hydrogen bromide, HBr, two products, 1-bromopropane and 2-bromopropane are formed. The reaction is a two-step process in which the electrophilic attack occurs in the first step. Identify the electrophile in this reaction Draw a diagram showing the first step of the reaction that leads to the production of 2-bromopropane.H3C CH3 H3C NA C→XT Br Br₂ CH₂Cl₂ H3C Electrophilic addition of bromine, Br₂, to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH₂Cl₂. CH3 Br In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due to steric clashes, the bromide ion always attacks the carbon from the opposite face of the bromonium ion so that a product with anti stereochemistry is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions Br CH3 H3C CH3Provide the structure for all major products of the following reactions. OCH3 он R O,N" NH2 NaOH H3C°
- Which of the following alkene reactions has a charged, cyclic reactive intermediate? Hydroboration Hydration Hydrohalogenation Halogenation Catalytic hydrogenationWhat reagents are needed to carry out this reaction? CH;CH,CH2CCH PCC in methylene chloride Sia2BH and then basic hydrogen peroxide Aqueous acid and mercury sulfate MCPBA and then Swern Oxidation Question 10 What is the intermediate that forms during this reaction? CH;CH,CH,CCH O an enol an epoxide an alkoxide a carbanionThe SN2 reaction is an example of a nucleophilic substitution reaction. Draw the structure of the two reactants and the mechanism of the reaction. The reaction is 1-bromo-3-ethylpentane reacts with cyclohexanol under basic conditions.