Start with the condensed structural formula CH3-CH=CH-CH2-CH3, and react it first with H20 in the presence of H2SO4 (as the catalyst), to produce TWO major substrate products. Then, take those two major substrate products, and use them as the substrates of the next reaction, by reacting each with K2Cr2O7 and H2SO4, to produce TWO FINAL MAJOR substrate products. [There are a total of two final major substrate products, not four.]

Start with the condensed structural formula CH3-CH=CH-CH2-CH3, and react it first with H20 in the presence of H2SO4 (as the catalyst), to produce TWO major substrate products. Then, take those two major substrate products, and use them as the substrates of the next reaction, by reacting each with K2Cr2O7 and H2SO4, to produce TWO FINAL MAJOR substrate products. [There are a total of two final major substrate products, not four.]

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter10: Organohalides

Section10.SE: Something Extra

Problem 19MP: The formation of Br2 from NBS first involves the reaction of NBS with HBr to form an iminol...

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Start with condensed structural formula CH3-CH(OH)-CH(CH3)-CH2-CH(CH3)2 and react it first with H2SO4 and high heat, to produce a major substrate product. Then, take that major substrate product, and use it as the substrate of the next reaction, by reacting it with Br2 (in the presence of CH2Cl2 solvent), to produce the FINAL MAJOR substrate product. The complete correct condensed structural formula for the major substrate product after reaction step 1 is ___________. (If no new product is formed in this step, type "no reaction.") The complete correct condensed structural formula for the final major substrate product (after reaction step 2) is __________ . (If no new product is formed in this step, type "no reaction.")
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