Chapter 11: Q17P (page 559)
When cis-2-methylcyclohexanol reacts with the Lucas reagent, the major product is 1-chloro-1-methylcyclohexane. Propose a mechanism to explain the formation of this product.
Chapter 11: Q17P (page 559)
When cis-2-methylcyclohexanol reacts with the Lucas reagent, the major product is 1-chloro-1-methylcyclohexane. Propose a mechanism to explain the formation of this product.
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Get started for freeUnder acid catalysis, tetrahydrofurfuryl alcohol reacts to give surprisingly good yields of dihydropyran. Propose a mechanism to explain this useful synthesis.
Contrast the mechanism of the two preceding reactions, the dehydration and condensation of ethanol.
We have covered several oxidants that use a multi-valent atom (Cr, Cl, S, or I) as their active species, going from a higher oxidation state before the oxidation to a lower oxidation state after oxidizing the alcohol. Draw the structure of the following atoms, before and after the oxidation of an alcohol to a ketone or aldehyde. How many bonds to oxygen does each atom have before and after the oxidation?
(a) the Cr in chromic acid
(b) the Cl in sodium hypochlorite
(c) the S in the Swern oxidation
(d) the I in the DMP reagent
(e)the carbinol C in the alcohol that is oxidized.
Two unknowns, X and Y, both having the molecular formula C4H8O , give the following results with four chemical tests. Propose structures for X and Y consistent with this information.
Bromine | Na metal | Chromic acid | Lucas reagent | |
Compound X | decolorizes | Bubbles | orange to green | no reaction |
Compound Y | no reaction | no reaction | no reaction | no reaction |
The following reaction involves a starting material with a double bond and a hydroxyl group, yet its mechanism resembles a pinacol rearrangement. Propose a mechanism, and point out the part of your mechanism that resembles a pinacol rearrangement.
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