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Which of these structures has the least number of monochlorination products?
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- HOW MANY different monochlorination products (disregarding stereoisomers) are produced in the following reaction?When bromine is added to two beakers, one containing phenyl isopropyl ether and the other containing cyclohexene, the bromine color in both beakers disappears. What observation could you make while performing this test that would allow you to distinguish the alkene from the aryl ether?Name and draw structural formulas for all possible monochlorination products that might be formed in each reaction.
- What are the major and minor products formed when cyclohexene reacts with Br2 in the solvent CH2Cl2?The reaction of 3-methylene-1-cyclohexene and HBr yields the four products shown in the attachment. Which two are formed at high temperatures and which two are formed at low temperatures? Why? Why is 1-bromo-3-methylenecyclohexane not formed?Explain the role strain plays on stability and reactivity of a cyclic alkane such as cyclopropane.
- An alkylbromide [X] produces single alkene[Y] when it reacts with sodium ethoxide and ethanol. [Y] upon hydrogenation produces 2-methylbutane. Choose the correct statement(s) among the following [X] is a tertiary alky bromide [X] is a primary alky bromide [X] may or may not show stereoisomerism [Y] can exhibit geometrical isomerismName the product formed after 1-chloroheptane 1) undergoes elimination then 2) reacts with HBr. Disregard stereochemistry.Which of these statements is true about halogenation of 2-methylbutane? It occurs via an addition reaction. B The primary C is halogenated first. Based on probability, the dominant product should be a tertiary alkylhalide. None of the choices