он Нас CH3 H3C CH3 Cr(VI) compounds are common reagents for the oxidation of alcohols. Primary alcohols are oxidized to carboxylic acids and secondary alcohols are oxidized to ketones. The mechanism involves a reaction similar to the E2 elimination, whereby a C=O double bond is formed with a reduced Cr(IV) compound as the leaving group Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions O: H3CCCH3

Organic Chemistry
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ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter19: Aldehydes And Ketones: Nucleophilic Addition Reactions
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Problem 36MP: It is not uncommon for organic chemists to prepare acetals by an exchange-type process known as...
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Cr(VI) compounds are common reagents for the oxidation of alcohols. Primary alcohols are oxidized to carboxylic acids and secondary alcohols are oxidized to ketones. The mechanism involves a reaction similar to the E2 elimination, whereby a C=O double bond is formed with a reduced Cr(IV) compound as the leaving group.

Draw curved arrows to show the movement of electrons in this step of the mechanism.

он
Нас
CH3
H3C
CH3
Cr(VI) compounds are common reagents for the oxidation of alcohols. Primary alcohols are oxidized to carboxylic acids and secondary alcohols are oxidized to
ketones. The mechanism involves a reaction similar to the E2 elimination, whereby a C=O double bond is formed with a reduced Cr(IV) compound as the leaving
group
Draw curved arrows to show the movement of electrons in this step of the mechanism.
Arrow-pushing Instructions
O:
H3CCCH3
Transcribed Image Text:он Нас CH3 H3C CH3 Cr(VI) compounds are common reagents for the oxidation of alcohols. Primary alcohols are oxidized to carboxylic acids and secondary alcohols are oxidized to ketones. The mechanism involves a reaction similar to the E2 elimination, whereby a C=O double bond is formed with a reduced Cr(IV) compound as the leaving group Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions O: H3CCCH3
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