Question

RM-Q19 Chloroacetic acid, CICH2CO2H, is a stronger acid than acetic acid. Which one of the following best explains this? Sele
RM-247 Which of the synthetic procedures below would carry out the following transformation? OH H ? H3C CH3 H3C CH; A) LiAlH,
RM-Q20 The compound shown below is classified as a(n) Select an answer and submit. For keyboard navigation, use the up/down a
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Answer #1

RM-Q19

Answer:

ClCH2CO2- is more stable than CH3CO2- because of the electron-withdrawing Cl.

Hence, Option a ClCH2CO2- is more stable than CH3CO2- because of the electron-withdrawing Cl is the correct answer.

Explanation:

Chloroacetic acid, ClCH2CO2H is stronger acid than acetic acid, CH3CO2H because the conjugate base of Chloroacetic acid, ClCH2CO2- is more stable due to electron-withdrawing effeect of Cl that reduces the electron density above oxygen atom whereas the conjugate base of acetic acid, CH3CO2- is less stable as it has no such effect.

RM-Q47

Answer:

Best reagent is D) NaBH4/methanol followed by HIO4.

Hence, Option C. D is the correct answer.

Explanation (mechanism):

HO HO =0 HO HO. HO: Ho: NaBH_/methanol HIO4 [H] 0 CH3 CH3 CH3 -CH3 CH3 CH3 0o OH HO H ولز + H H -CH3 CH3 CH3 Product CH3

RM-Q20

Answer:

The compound shown below is classified as a Carboxylic Anhydride.

Hence, Option b Carboxylic Anhydride is the correct answer.

Explanation:

O O R = Alkyl group R= Alkyl group R R H OR beta ketoester carboxylic anhydride OH OH vi R= Alkyl group ün R= Alkyl group R R

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