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- C10T05Q3420 Give the major organic product for the following reaction. H H H catalytic heat if There is no reaction under these conditions or the correct product is not listed here.Which will yield 2-methylpentane upon catalytic hydrogenation?Which of these alkyl chlorides undergoes dehydrohalogenation in the presence of a strong base to give pent-2-ene (shown below) as the only alkene product? O l-chloro-2-methylbutane O 2-chloropentane O 3-chloropentane O 1-chloropentane O l-chloro-3-methylbutane
- Which represents an efficient synthetic route to go from an alkane to an alkene? O elimination with NaNH2, followed by a water workup O anti-Markovnikov hydrohalogenation, followed by elimination O radical bromination, followed by elimination O hydration, followed by elimination O hydration, followed by ozonolysis of the double bondwhat is the structure of the substitution product in the following reaction and consider stereochemistry in deciding your product?Draw a structure for the product of nucleophilic substitution obtained on solvolysis of tert-butyl bromide in methanol, and arrange the correct mechanism for its formation. Be sure to answer all parts.
- 58) Draw the product resulting from the following reaction. Indicate any relevant stereo chemistry. Eto EtOHWhat is(are) the product(s) in the Pd-catalyzed hydrogenation of 1,2-dimethylcyclopentene? Include stereochemistry.1) What is the major product generally formed when a tertiary alkyl bromide (R3Br) reacts with sodium methoxide in methanol? 2) How is this major product formed?