What is the correct name for the following compound? Br (R)-3-bromo-3-methoxyprop-1-ene (R,S)-taylorswiftistonedeaf-3-ol (S)-3-bromo-3-methoxyprop-1-ene (S)-3-bromo-3-methoxyprop-2-ene (R)-2-bromo-2-methoxyprop-1-ene For an acid/base reaction to be unsuccessful (ie to NOT proceed in the direction of products to any great extent).. The conjugate base should be weaker than the parent base None of these is true The conjugate acid should be stronger than the parent acid Only resonance stabilisation of reactants is required Only resonance stabilisation of products is required

What is the correct name for the following compound? Br (R)-3-bromo-3-methoxyprop-1-ene (R,S)-taylorswiftistonedeaf-3-ol (S)-3-bromo-3-methoxyprop-1-ene (S)-3-bromo-3-methoxyprop-2-ene (R)-2-bromo-2-methoxyprop-1-ene For an acid/base reaction to be unsuccessful (ie to NOT proceed in the direction of products to any great extent).. The conjugate base should be weaker than the parent base None of these is true The conjugate acid should be stronger than the parent acid Only resonance stabilisation of reactants is required Only resonance stabilisation of products is required

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter7: Alkenes: Structure And Reactivity

Section7.SE: Something Extra

Problem 62AP: The heat of hydrogenation for allene (Problem 7-61) to yield propane is -295 kJ/mol, and the heat of...

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In 4+2 cycloaddition, ENDO stereochemistry is preferred because: endo stereochemistry allows the diene to adopt s-cis conformation. endo stereochemistry results in less steric hindrance. the transition state leading to endo stereochemistry is higher energy. it allows for additional π to π overlap between the diene and the dienophile.
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