40 the C =0 bond?A. The oxygen atom is partially reactive due to the strong bond dipole.B. The carbon atom does not form a highly polar bond with hydrogen.C. The oxygen atom is sp² hybridized with almost 67% p character.D. Oxygen exhibits resonance with carbon leading to bond stability.40. What is the role of H+ ions in the nucleophilic substitution of alcohols using hydrogen halides?A. Protonation of -OH groupB. Stabilization of carbocationC. Activation of oxygen radicalD. Removal of an alkyl group

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40. What is the role of H+ ions in the nucleophilic substitution of alcohols using hydrogen halides? A. Protonation of -OH group B. Stabilization of carbocation C. Activation of oxygen radical D. Removal of an alkyl group

40. What is the role of H+ ions in the nucleophilic substitution of alcohols using hydrogen halides? A. Protonation of -OH group B. Stabilization of carbocation C. Activation of oxygen radical D. Removal of an alkyl group

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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Concept explainers

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.

Question

the C =0 bond?
A. The oxygen atom is partially reactive due to the strong bond dipole.
B. The carbon atom does not form a highly polar bond with hydrogen.
C. The oxygen atom is sp² hybridized with almost 67% p character.
D. Oxygen exhibits resonance with carbon leading to bond stability.
40. What is the role of H+ ions in the nucleophilic substitution of alcohols using hydrogen halides?
A. Protonation of -OH group
B. Stabilization of carbocation
C. Activation of oxygen radical
D. Removal of an alkyl group

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