19.3 Preparing Aldehydes and Ketones: A Review Predict the major product of the following reaction. OH HO CrO₂ H₂SO4 OH OH There is no reaction under these conditions or the correct product is not listed here.

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19.3 Preparing Aldehydes and Ketones: A Review
Predict the major product of the following reaction.
OH
O
O
HO
20
OH
There is no reaction under these conditions or the correct product is not listed here.
19.5 Oxygen Nucleophiles
CrO₂
H₂SO4
?
In the mechanism for acetal formation, the second step is a:
19.9 Hydrogen Nucleophiles
OH
O nucleophilic attack.
deprotonation of its oxonium ion.
proton transfer.
loss of its leaving group.
O acetophenone.
Ophenol.
O cyclohexanol.
Obenzyl alcohol.
Identify the product expected when the following compound is treated with LiAlH4 followed by water.
O acetophenone.
Ohexanone.
O cyclohexanone.
O benzyl alcohol.
Obenzaldehyde.
Ocyclopentanone.
19.11 Baeyer-Villiger Oxidation of Aldehydes and Ketones
Which of the following compounds can be directly converted into the lactone shown via a Baeyer-Villiger oxidation?
с
A
SI
Transcribed Image Text:19.3 Preparing Aldehydes and Ketones: A Review Predict the major product of the following reaction. OH O O HO 20 OH There is no reaction under these conditions or the correct product is not listed here. 19.5 Oxygen Nucleophiles CrO₂ H₂SO4 ? In the mechanism for acetal formation, the second step is a: 19.9 Hydrogen Nucleophiles OH O nucleophilic attack. deprotonation of its oxonium ion. proton transfer. loss of its leaving group. O acetophenone. Ophenol. O cyclohexanol. Obenzyl alcohol. Identify the product expected when the following compound is treated with LiAlH4 followed by water. O acetophenone. Ohexanone. O cyclohexanone. O benzyl alcohol. Obenzaldehyde. Ocyclopentanone. 19.11 Baeyer-Villiger Oxidation of Aldehydes and Ketones Which of the following compounds can be directly converted into the lactone shown via a Baeyer-Villiger oxidation? с A SI
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