Compound x (CeH12 reacts with BH3 followed by H2O2. NaOH, H20 to yield Compound Y (CgH140) as the major organic product. When Y is exposed to the reaction conditions that should be listed in Box z. the carboxylic acid product shown forms as the major product. The IR spectrum of X has prominent absorptions at 3079 cm-1 and at 1643 cm-1. The 'H NMR spectrum of X shows signals at 8 0.90 (d, 6H), 1.63 (m, 1H), 1.94 (dd, 2H), 4.96 (m, 1H), 4.97 (m, 1H), and 5.77 (m, 1H). The 13C NMR spectrum of X shows signals at 5 22.3, 28.2, 43.5, 115.4, and 137.9. Deduce the structures of Compound X and Compound Y, and indicate the yeaction conditions that should be written in Box Z. 1) BH, 2) H,O, N2OH, HO X (C,H12) Y (C,H140)
Compound x (CeH12 reacts with BH3 followed by H2O2. NaOH, H20 to yield Compound Y (CgH140) as the major organic product. When Y is exposed to the reaction conditions that should be listed in Box z. the carboxylic acid product shown forms as the major product. The IR spectrum of X has prominent absorptions at 3079 cm-1 and at 1643 cm-1. The 'H NMR spectrum of X shows signals at 8 0.90 (d, 6H), 1.63 (m, 1H), 1.94 (dd, 2H), 4.96 (m, 1H), 4.97 (m, 1H), and 5.77 (m, 1H). The 13C NMR spectrum of X shows signals at 5 22.3, 28.2, 43.5, 115.4, and 137.9. Deduce the structures of Compound X and Compound Y, and indicate the yeaction conditions that should be written in Box Z. 1) BH, 2) H,O, N2OH, HO X (C,H12) Y (C,H140)
Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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![Compound X (CeH12 reacts with BH3 followed by H202. NaOH, H2O to yield Compound Y (CgH140) as the major organic product. When Y is exposed to the reaction conditions
that should be listed in Box z, the carboxylic acid product shown forms as the major product.
The IR spectrum of X has prominent absorptions at 3079 cm-1 and at 1643 cm-1.
The 'H NMR spectrum of X shows signals at 8 0.90 (d, 6H), 1.63 (m, 1H), 1.94 (dd, 2H), 4.96 (m, 1H), 4.97 (m, 1H), and 5.77 (m, 1H).
The 13C NMR spectrum of X shows signals at 8 22.3, 28.2, 43.5, 115.4, and 137.9.
Deduce the structures of Compound X and Compound Y, and indicate the reaction conditions that should be written in Box Z.
Z
1) BH,
HO
2) H,0 NaOH, ңо
X (C,H12)
Y (C,H140)](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F4783cb6f-c9a6-486a-a4d0-5a07a49ff57e%2Ff04fcb41-1248-4019-b012-e74f64d3811c%2Fnc9qy3l_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Compound X (CeH12 reacts with BH3 followed by H202. NaOH, H2O to yield Compound Y (CgH140) as the major organic product. When Y is exposed to the reaction conditions
that should be listed in Box z, the carboxylic acid product shown forms as the major product.
The IR spectrum of X has prominent absorptions at 3079 cm-1 and at 1643 cm-1.
The 'H NMR spectrum of X shows signals at 8 0.90 (d, 6H), 1.63 (m, 1H), 1.94 (dd, 2H), 4.96 (m, 1H), 4.97 (m, 1H), and 5.77 (m, 1H).
The 13C NMR spectrum of X shows signals at 8 22.3, 28.2, 43.5, 115.4, and 137.9.
Deduce the structures of Compound X and Compound Y, and indicate the reaction conditions that should be written in Box Z.
Z
1) BH,
HO
2) H,0 NaOH, ңо
X (C,H12)
Y (C,H140)
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