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Treatment of 2-Hexanone with NaOCH2CH3 Followed by CH3Br Affords Compound

Question 22

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Treatment of 2-hexanone with NaOCH2CH3 followed by CH3Br affords compound X (C7H14O) as the major product.X shows a strong absorption in the IR spectrum at 1713 cm-1,and its 1H NMR data is given below.What is the structure of X? Treatment of 2-hexanone with NaOCH<sub>2</sub>CH<sub>3</sub> followed by CH<sub>3</sub>Br affords compound X (C<sub>7</sub>H<sub>14</sub>O) as the major product.X shows a strong absorption in the IR spectrum at 1713 cm<sup>-1</sup>,and its <sup>1</sup>H NMR data is given below.What is the structure of X? A) I B) II C) III D) IV Treatment of 2-hexanone with NaOCH<sub>2</sub>CH<sub>3</sub> followed by CH<sub>3</sub>Br affords compound X (C<sub>7</sub>H<sub>14</sub>O) as the major product.X shows a strong absorption in the IR spectrum at 1713 cm<sup>-1</sup>,and its <sup>1</sup>H NMR data is given below.What is the structure of X? A) I B) II C) III D) IV Treatment of 2-hexanone with NaOCH<sub>2</sub>CH<sub>3</sub> followed by CH<sub>3</sub>Br affords compound X (C<sub>7</sub>H<sub>14</sub>O) as the major product.X shows a strong absorption in the IR spectrum at 1713 cm<sup>-1</sup>,and its <sup>1</sup>H NMR data is given below.What is the structure of X? A) I B) II C) III D) IV


A) I
B) II
C) III
D) IV

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