3.1. Draw structure of a tertiary alcohol with four carbons, give its IUPAC name and then show the REACTION MECHANISM for the formation of an alkyl halide from this alcohol. HINT: - The reaction is Sw1, it takes place through 3 STEPS and TWo carbocations forms as intermediates. - The reaction was carried in the presence of an acid and in the presence of halide ions, and not at elevated temperature. - Halide ions are good nucleophiles (they are much stronger nucleophiles than water), and since halide ions are present in high concentration, most of the carbocations react with an electron pair of a halide ion to form a more stable species, the alkyl halide product. - OH group is a poor leaving group, thus the alcohol gets protonated first. STRUCTURE OF A TERTIARY ALCOHOL IUPAC NAME REACTION MECHANISM

3.1. Draw structure of a tertiary alcohol with four carbons, give its IUPAC name and then show the REACTION MECHANISM for the formation of an alkyl halide from this alcohol. HINT: - The reaction is Sw1, it takes place through 3 STEPS and TWo carbocations forms as intermediates. - The reaction was carried in the presence of an acid and in the presence of halide ions, and not at elevated temperature. - Halide ions are good nucleophiles (they are much stronger nucleophiles than water), and since halide ions are present in high concentration, most of the carbocations react with an electron pair of a halide ion to form a more stable species, the alkyl halide product. - OH group is a poor leaving group, thus the alcohol gets protonated first. STRUCTURE OF A TERTIARY ALCOHOL IUPAC NAME REACTION MECHANISM

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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