Compound A has molecular formula C7H7X. Its ¹H-NMR spectrum shows a singlet at 2.26 ppm and two doublets, one at 6.95 ppm and one at 7.28 ppm. The singlet has an integral of three and the doublets each have an integral of two. Its 13C-NMR shows five signals. The mass spectrum of A shows a peak at m/z = 170 and another peak at m/z = 172; the relative height of the two peaks is 1:1 respectively. - Identify what atom X is, explaining your reasoning - Identify Compound A, explaining your reasoning Compound A is treated with a mixture of nitric and sulfuric acids to generate Compound B. The ¹H-NMR spectrum of B shows two singlets, one at 2.52 pm and one at 8.13 ppm. The 13C-NMR spectrum of B shows five signals. The mass spectrum of B shows a peak at m/z = 260 and another peak at m/z = 262; the relative height of the two peaks is 1:1 respectively. - Identify compound B, explaining your reasoning Compound B is treated with sodium ethoxide to generate compound C. The ¹H-NMR spectrum of C shows four signals - a triplet at 1.24 ppm, a singlet at 2.32 ppm, a quartet at 4.14 ppm, and a singlet at 7.42 ppm. The 13C-NMR spectrum of C shows seven signals. - Identify compound C, explaining your reasoning

Compound A has molecular formula C7H7X. Its ¹H-NMR spectrum shows a singlet at 2.26 ppm and two doublets, one at 6.95 ppm and one at 7.28 ppm. The singlet has an integral of three and the doublets each have an integral of two. Its 13C-NMR shows five signals. The mass spectrum of A shows a peak at m/z = 170 and another peak at m/z = 172; the relative height of the two peaks is 1:1 respectively. - Identify what atom X is, explaining your reasoning - Identify Compound A, explaining your reasoning Compound A is treated with a mixture of nitric and sulfuric acids to generate Compound B. The ¹H-NMR spectrum of B shows two singlets, one at 2.52 pm and one at 8.13 ppm. The 13C-NMR spectrum of B shows five signals. The mass spectrum of B shows a peak at m/z = 260 and another peak at m/z = 262; the relative height of the two peaks is 1:1 respectively. - Identify compound B, explaining your reasoning Compound B is treated with sodium ethoxide to generate compound C. The ¹H-NMR spectrum of C shows four signals - a triplet at 1.24 ppm, a singlet at 2.32 ppm, a quartet at 4.14 ppm, and a singlet at 7.42 ppm. The 13C-NMR spectrum of C shows seven signals. - Identify compound C, explaining your reasoning

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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essibility 12 + B I U A Q Search 1 1. Cobalt System (watch video) [Co(H,O)]*(aq) + 4CI Pink Stress None (CONTROL) Addition of H₂O Addition of HCI Add heat 1 Remove heat Addition of =-=-=-=-33 X 2 = NaCl Initial Color: Observations (Color Change?) L (aq) 31 + heat → [COCI]² (aq) + 6H₂O(1) KE Blue Notes: Sodium ions react with chloride ions to form the insoluble precipitate Table options Explain using Le Chatelier's Principle
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Which atom is the most nucleophilic? C
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