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- What is/are the product/products of this reaction? NBS ROOR ? CH3 Br CH2 -Br CH2BR CH3 Br- CH2 CH,Br Br +Consider the dehydration reaction of 2-methyl-hexan-2-ol. How many different alkenes will be produced by this reaction? (Hint: name each of your products to be sure that no two are the same compound.) 3 2 1 5 4The reaction of Hbr with 2-methylpropene produces 2-bromo-2-methylpropane. What is the structure of the carbocation formed during the reaction?
- CH3COOH + 2H2 = C2H5OH + H2O %3D Acetate Ethanol Acetate may be hydrogenated to ethanol in industrial reaction systems using several catalysts: Select the most effective catalyst for this reaction system if the free energy of the reaction is -34 kJ/mol; Catalist effective at the temperature range 37-45°C, O Catalist effective at the temperature range 40-55°C, O Catalist effective at the temperature range 60-72°C,Cyclopropane decomposes fairly rapidly at moderate temperatures whereas cyclohexane is quite stable. Why is this the case?Fill in the missing product (R) а меона меон b* H*, H₂O CO₂Me CO₂Me a Na toluene bH, H₂O
- Name the major product of the reaction between (S)-2-bromohexane and KCH3COO. Be specific with the configuration. Name the alcohol that will produce the most stable intermediate and the dehydration product 2-methyl-1,3-pentadiene.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 two possible carbocations that can form when this alkene reacts with a strong acid (such as HBr or H3O+). of the two structures you drew, circle the more stable carbocation