9. (a) Under certain conditions, the reaction of 0.5 M 1-bromobutane with 1.0 M sodium methoxide forms 1-methoxybutane at a rate of 0.05 mol/L per second. What would be the rate if 0.1 M 1-bromobutane and 2.0 M NaOCH3 were used? (b) Consider the reaction of 1-bromobutane with a large excess of ammonia (NH3). Draw the reactants, the transition state, and the products. Note that the initial product is the salt of an amine (RNH+ Br) which is deprotonated by the excess ammonia to give the amine. (c) Show another SN2 reaction using a different combination of an alkoxide and an alkyl bromide that also produces 1-methoxybutane.
9. (a) Under certain conditions, the reaction of 0.5 M 1-bromobutane with 1.0 M sodium methoxide forms 1-methoxybutane at a rate of 0.05 mol/L per second. What would be the rate if 0.1 M 1-bromobutane and 2.0 M NaOCH3 were used? (b) Consider the reaction of 1-bromobutane with a large excess of ammonia (NH3). Draw the reactants, the transition state, and the products. Note that the initial product is the salt of an amine (RNH+ Br) which is deprotonated by the excess ammonia to give the amine. (c) Show another SN2 reaction using a different combination of an alkoxide and an alkyl bromide that also produces 1-methoxybutane.
Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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![9. (a) Under certain conditions, the reaction of 0.5 M 1-bromobutane with 1.0 M sodium
methoxide forms 1-methoxybutane at a rate of 0.05 mol/L per second. What would be the
rate if 0.1 M 1-bromobutane and 2.0 M NaOCH3 were used?
(b) Consider the reaction of 1-bromobutane with a large excess of ammonia (NH3). Draw
the reactants, the transition state, and the products. Note that the initial product is the salt
of an amine (RNH* Br) which is deprotonated by the excess ammonia to give the amine.
(c) Show another SN2 reaction using a different combination of an alkoxide and an alkyl
bromide that also produces 1-methoxybutane.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fa0ad014c-1e99-4925-ac0a-7b6dd706a94e%2Fafecfb1a-8598-4b09-9b4e-673ccd66511d%2F8ksogsb_processed.jpeg&w=3840&q=75)
Transcribed Image Text:9. (a) Under certain conditions, the reaction of 0.5 M 1-bromobutane with 1.0 M sodium
methoxide forms 1-methoxybutane at a rate of 0.05 mol/L per second. What would be the
rate if 0.1 M 1-bromobutane and 2.0 M NaOCH3 were used?
(b) Consider the reaction of 1-bromobutane with a large excess of ammonia (NH3). Draw
the reactants, the transition state, and the products. Note that the initial product is the salt
of an amine (RNH* Br) which is deprotonated by the excess ammonia to give the amine.
(c) Show another SN2 reaction using a different combination of an alkoxide and an alkyl
bromide that also produces 1-methoxybutane.
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