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Purpose of Experiment: The purpose 6E the experiment is to provde an example of a reacthion of an organometallic feaetion heagent with an aldehude to prepare an aichol I. II. Reactions carried out: G3H3BZQNHI ÇI Hao, THẾ Br Ha 0,THF Zn, N tyCI znB-(WHs)a П. Data Isolated yield of product: Theoretical yield of adduct: Percent yield of adduct: IV. Questions 1. Normally, most organometallics are very sensitive to water and even trace amounts can prevent their formation. What is the predominant reaction of organometallics with water? (Write the general reaction beginning with R-Metal + H2O →) 2. Draw the structures of the product of the reaction of each of the organometallics below with water. a. butyllithium b. phenylmagnesium bromide c. lithium dicyclohexylcuprate(I) 3. Draw the structures of the product of the reaction of each of the organometallics below with D20. a. butyllithium b. phenylmagnesium bromide c. lithium dicyclohexylcuprate(I) 11

Purpose of Experiment: The purpose 6E the experiment is to provde an example of a reacthion of an organometallic feaetion heagent with an aldehude to prepare an aichol I. II. Reactions carried out: G3H3BZQNHI ÇI Hao, THẾ Br Ha 0,THF Zn, N tyCI znB-(WHs)a П. Data Isolated yield of product: Theoretical yield of adduct: Percent yield of adduct: IV. Questions 1. Normally, most organometallics are very sensitive to water and even trace amounts can prevent their formation. What is the predominant reaction of organometallics with water? (Write the general reaction beginning with R-Metal + H2O →) 2. Draw the structures of the product of the reaction of each of the organometallics below with water. a. butyllithium b. phenylmagnesium bromide c. lithium dicyclohexylcuprate(I) 3. Draw the structures of the product of the reaction of each of the organometallics below with D20. a. butyllithium b. phenylmagnesium bromide c. lithium dicyclohexylcuprate(I) 11

Chemistry
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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Purpose of Experiment: The purpose 6E the experiment is to provde an example of a reacthion of an organometallic feaetion heagent with an aldehude to prepare an aichol I. II. Reactions carried out: G3H3BZQNHI ÇI Hao, THẾ Br Ha 0,THF Zn, N tyCI znB-(WHs)a П. Data Isolated yield of product: Theoretical yield of adduct: Percent yield of adduct: IV. Questions 1. Normally, most organometallics are very sensitive to water and even trace amounts can prevent their formation. What is the predominant reaction of organometallics with water? (Write the general reaction beginning with R-Metal + H2O →) 2. Draw the structures of the product of the reaction of each of the organometallics below with water. a. butyllithium b. phenylmagnesium bromide c. lithium dicyclohexylcuprate(I) 3. Draw the structures of the product of the reaction of each of the organometallics below with D20. a. butyllithium b. phenylmagnesium bromide c. lithium dicyclohexylcuprate(I) 11
Transcribed Image Text:Purpose of Experiment: The purpose 6E the experiment is to provde an example of a reacthion of an organometallic feaetion heagent with an aldehude to prepare an aichol I. II. Reactions carried out: G3H3BZQNHI ÇI Hao, THẾ Br Ha 0,THF Zn, N tyCI znB-(WHs)a П. Data Isolated yield of product: Theoretical yield of adduct: Percent yield of adduct: IV. Questions 1. Normally, most organometallics are very sensitive to water and even trace amounts can prevent their formation. What is the predominant reaction of organometallics with water? (Write the general reaction beginning with R-Metal + H2O →) 2. Draw the structures of the product of the reaction of each of the organometallics below with water. a. butyllithium b. phenylmagnesium bromide c. lithium dicyclohexylcuprate(I) 3. Draw the structures of the product of the reaction of each of the organometallics below with D20. a. butyllithium b. phenylmagnesium bromide c. lithium dicyclohexylcuprate(I) 11
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