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- CH3 CH3 H cyclopentamine The synthesis of cyclopentamine, an amphetamine-like central nervous system stimulant, from materials of five carbons or fewer involves several steps, one of which is shown below. Draw the structure(s) of the major organic product(s) of the following reaction: Mg, dry ether Br productWhen 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.Diazomethane, CH2N2, is used in the organic chemistry laboratory despite its danger because it produces very high yields and is selective for reaction with carboxylic acids. Write the products of the following reactions.
- 2) What is the product of the following reaction? HBr Br₂ H₂O 3) Write the product of the following reaction. CH₂OHGive the major organic product(s) for each of the following reactions. Write NR if a reaction will not occur.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.
- Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium with their conjugated , -unsaturated isomers. Propose a mechanism for this isomerization.Complete the following sequence of reactions by drawing the structures of compounds A through D. Hint: Compound D has the molecular formula C5H8O4 O || HỌ–CH,CH,CNH, Compound A Compound B Compound C+ 2 CH₂-OH! Hydrolysis (pH 1) Oxidation Oxidation Condensation Compound A+ NH₂* Compound B Compound C Compound D + 2 H₂OReaction of (CH3)3CH with Cl2 forms two products: (CH3)2CHCH2Cl (63%) and (CH3)3CCl (37%). Why is the major product formed by cleavage of the stronger 1° C–H bond?
