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- 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 CH3Draw the alkene that would react with the reagent given to account for the product formed. ? + HCI My 3 You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. CH3 CH₂ CHOCH3 TT CI CH3 L ▼ {n [F ? ChemDoodleⓇWhat are the major and minor products formed when cyclohexene reacts with Br2 in the solvent CH2Cl2?
- When cyclohexene is reacted with hydrobromic acid in acetic acid, the major product is bromocyclohexane. There is a small amount of cyclohexyl acetate formed. What is the mechanism that forms both compounds? What is the purification procedure that isolates both compounds?acetone H3C, HO H3C OH The product of the following reaction is: A OH H3C OH C D OB2. What is the product of the following reaction? کہا NaOH, H₂O A
- Draw the two reactants used to form the following compound, label the nucleophile and the electrophile, and using arrows show the points of attack of the nucleophile on the electrophile that enables the formation of the heterocyclic product.Which alcohol will form the most stable carbocation? CH3 a) CH;CHCH,OH CH3 b) CH—сон CH3 c) - OH d) CH;OH O a O b O d Organic compounds that contain terminal carbonyl group. ketone aldehyde ether alcoholWhat is the product of the following reaction sequence? II CH;CH2CCH; Но* Mg CH;CH2CH2B O 3-methyl-3-hexanol O 2-methyl-3-hexanol 3-ethyl-2-pentanol 2-heptanol