The cyclobutenyl dichloride deriviative below reacts with the powerful Lewis acid antimonypentafluoride in liquid SO₂ at -75° to give a pale yellow solution that exhibits one singlet at 3.68 ppmin its ¹H-NMR spectrum. The species in solution (A) has been identified as the salt C8H₁2X2 where X isan hexahaloantimonate anion. Draw the structure of the C8H12 ion.H3COH3C●H3C.H₂CCH3m...• Draw cations and anions in separate sketchers.Separate structures with + signs from the drop-down menu.CH3CI-CICH3CH3SbF5SO2, -75°?C8H12X2(X= hexahaloantimonate anion)Sn [FOSb-F-ClPrevious?Next

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The cyclobutenyl dichloride deriviative below reacts with the powerf pentafluoride in liquid SO₂ at -75° to give a pale yellow solution that exhibits one singlet at 3.68 ppm in its ¹H-NMR spectrum. The species in solution (A) has been identified as the salt C8H12X2 where X i an hexahaloantimonate anion. Draw the structure of the C8H 12 ion. H3C H3C CH3 -CI -CI CH3 SbF5 SO₂, -75⁰ C8H12X2 (X= hexahaloantimonate anion)

The cyclobutenyl dichloride deriviative below reacts with the powerf pentafluoride in liquid SO₂ at -75° to give a pale yellow solution that exhibits one singlet at 3.68 ppm in its ¹H-NMR spectrum. The species in solution (A) has been identified as the salt C8H12X2 where X i an hexahaloantimonate anion. Draw the structure of the C8H 12 ion. H3C H3C CH3 -CI -CI CH3 SbF5 SO₂, -75⁰ C8H12X2 (X= hexahaloantimonate anion)

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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