Which reagent from the below the list should be used to effect the transformation shown?

1) L i A l H_{4} / E t_{2} O; 2) B r_{2} / H_{2} O; 3) K_{2} C O_{3} / H_{2} O

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O s O_{4} / K I O_{4} / H_{2} O / A c e t o n e

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1) (C O C l)_{2} / M e_{2} S O / E t_{3} N / - 60^{o} C; 2) N a B H_{4} / E t O H / △

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K_{2} C r_{2} O_{7} / H_{2} S O_{4} / H_{2} O / A c e t o n e

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Solution

The correct option is D $K_{2} C r_{2} O_{7} / H_{2} S O_{4} / H_{2} O / A c e t o n e$
$K_{2} C r_{2} O_{7} / H_{2} S O_{4} / H_{2} O / A c e t o n e$ oxidises a primary alcohol into carboxylic acid leaving behind all other groups intact as :

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