Which is the most appropriate reagent for the following oxidation reaction?
$C H_{3} - C H = C H - C H_{2} O H \to C H_{3} - C H = C H - C O O H$

K M n O_{4} / H_{2} S O_{4}

No worries! We‘ve got your back. Try BYJU‘S free classes today!

K M n O_{4} / N a O H

No worries! We‘ve got your back. Try BYJU‘S free classes today!

C r O_{3} / H C l / P y r i d i n e

No worries! We‘ve got your back. Try BYJU‘S free classes today!

C r O_{3} / A c e t o n e / H_{2} O

Right on! Give the BNAT exam to get a 100% scholarship for BYJUS courses

Open in App

Solution

The correct option is C $C r O_{3} / A c e t o n e / H_{2} O$
Because acyclic ketones are relatively stable to $C r (V I)$ oxidations, acetone is frequently used as the solvent for $C r (V I)$ oxidations of alcohols. In these reactions, a $C r O_{3} / H_{2} S O_{4} / H_{2} O$ mixture is slowly added to an acetone solution of the alcohol, or the alcohol is mixed with an acetone solution of $C r O_{3} / H 2 S O 4 / H 2 O .$

Suggest Corrections

Similar questions

C H_{3} - C H = C H - C H_{2} - O H | C H - C H_{3} ⟶ C H_{3} - C H = C H - C H_{2} - C O O H

C H_{3} - C H = C H - C O O H \to C H_{3} - C H = C H - C H_{2} O H

C H_{3} - C H = C H - C H O

C H_{3} - C H = C H - C O O H

C H_{3} - C H = C H - C H_{2} - O | | C - C H_{3} \to C H_{3} - C H = C H - C H_{2} - O | | C - O H

C H_{2} = C H - C H_{2} O H \to C H_{2} = C H - C H O

C H_{3} - C O O H \to C H_{3} C O N H_{2}

Join BYJU'S Learning Program