9. option C and D carbocations are secondary carbocation. so these carbocations

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9.

option C and D carbocations are secondary carbocation. so these carbocations tends to rearrange to form stable carbocation.

secondary carbocation rearranges to more stable tertiary carbocation.

we know, as migration affinity of -CH3 group is greater than -H.

so option C structure leads to the -CH3 shift and option D structure leads to the -H shift.

so option C is the answer.

10.

option C is the answer.

becasuse phosfate diester part contains R3 part which is positive charged ammonium part. so this more polar.

R1 and R2 are hydrofobic part in this structure.

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9) Whch of the ftss would most couily undeugo 1,2-hydride shift? (A) (CHhC HC-O-C-R2 Phospholipids of the general formula shown above are arranged in lipid bilayers visualized as follows polar heads The polar heads which are exposed to an aqucous environment represent the (A) fatty acid group Ri only (B) fatty acid groups Ri and R2 (C) phosphate diester function (D) carbonyl function of the carboxylic acid (E) glycerol backbone

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