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- M 6 write the principal product in a, c & e and the neccesary reactives for b, d & f in the following reactions :What is the expected major product of reacting cyclohexane carbaldehyde with (CH3)2NH?For each reaction, decide whether substitution or elimination (or both) is possible, andpredict the products you expect. Label the major products. chlorocyclohexane + NaOC(CH3)3 in (CH3)3COH
- Complete the flowchart by drawing the resulting structures of each reaction. A. B. C. D. E. F. G. H. I.Provide a reasonable arrow-pushing mechanism for Reaction 5b, and explain the the stereochemical outcome. 5d belowThe major product formed by addition of HBr to (CH3)2C=CH– CH=C(CH3)2 is the same at low and high temperature. Draw the structure of the major product, and explain why the kinetic and thermodynamic products are the same in this reaction.
- 2. How many substitution product/s is/are formed when metabromo anisole is treated with ammonia?A. 0-no reactionB. 1C. 2D. 3Q2. What are the products of the following reactions? Q3. 2-Bromopentane, when treated with alcoholic KOH yields a mixture of three alkenes A, B and C. Identify A, B and C. Which is predominant? When 3-methyl-1-butene is reacted with 9-borabicyclo[3.3.1]nonane, the "1-ol" product is formed. What is the detailed reactin scheme for the transformation? Describe the purification procedure.
- Reaction of 2° alcohol A with HCl forms three alkyl chlorides, all of which result from rearrangement of the 2° carbocation initially formed. Draw the structures of these products and a mechanism that illustrates how each is formed.N(CH2CH3)3 + HNO3 --------> a.) rewrite the reaction using bond-line structure of reagents and products of the reaction b.) supply the curved arrows explaining the mechanism of the reactionWhat order of reagents should be used to synthesize the following product from methylcyclopentane?(A) Br2(B) Br2, hv(C) KOH, heat