Homework Help is Here – Start Your Trial Now!
Science
Chemistry
Tasks 1. Complete the reactions shown in Figure 9 by providing structures of reactants and/or products in empty spaces as well as reagents and reaction conditions (solvent, temperature, etc.) above/below SN2 + electrophile nucleophile solvent OH OTs OK DMF, 0 °C Br CN Figure 9: Reactions 2. Draw the mechanism of formation of the organic products in the reaction shown in Figure 10. S + HCI .S 1 SH CI 75% 25% Figure 10: Mechanism

Tasks 1. Complete the reactions shown in Figure 9 by providing structures of reactants and/or products in empty spaces as well as reagents and reaction conditions (solvent, temperature, etc.) above/below SN2 + electrophile nucleophile solvent OH OTs OK DMF, 0 °C Br CN Figure 9: Reactions 2. Draw the mechanism of formation of the organic products in the reaction shown in Figure 10. S + HCI .S 1 SH CI 75% 25% Figure 10: Mechanism

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...
See similar textbooks
icon
Related questions
Question
**Learning Target 11** **Criteria for satisfactory score:** Reactants, products, and reagents that complete a reaction scheme must be correct. Curved arrow mechanisms may contain one minor error (wrong arrow, missing formal charge, etc.) **Tasks:** 1. Complete the reactions shown in **Figure 9** by providing structures of reactants and/or products in empty spaces as well as reagents and reaction conditions (solvent, temperature, etc.) above/below. - **Diagram Description:** - The blank spaces in the figure are labeled for "electrophile," "nucleophile," and "solvent." - The reaction scheme involves an SN2 reaction, leading to a product. - Below, a specific reaction is illustrated: - Conversion of an alcohol (OH) to tosylate (OTs) using KOt and DMF at 0°C. - Conversion of a molecule with an iodine group to one with a bromine group, finally to a cyanide group. - **Figure 9: Reactions** 2. Draw the mechanism of formation of the organic products in the reaction shown in **Figure 10**. - **Diagram Description:** - A molecular structure featuring an SH group at position 1 and Cl at position 7. - The reaction proceeds to form two products: one major product (75%) and one minor product (25%) along with HCl. - The major product features a five-membered ring with a sulfur atom, while the minor product also contains a five-membered ring with an additional substituent. - **Figure 10: Mechanism**
Transcribed Image Text:**Learning Target 11** **Criteria for satisfactory score:** Reactants, products, and reagents that complete a reaction scheme must be correct. Curved arrow mechanisms may contain one minor error (wrong arrow, missing formal charge, etc.) **Tasks:** 1. Complete the reactions shown in **Figure 9** by providing structures of reactants and/or products in empty spaces as well as reagents and reaction conditions (solvent, temperature, etc.) above/below. - **Diagram Description:** - The blank spaces in the figure are labeled for "electrophile," "nucleophile," and "solvent." - The reaction scheme involves an SN2 reaction, leading to a product. - Below, a specific reaction is illustrated: - Conversion of an alcohol (OH) to tosylate (OTs) using KOt and DMF at 0°C. - Conversion of a molecule with an iodine group to one with a bromine group, finally to a cyanide group. - **Figure 9: Reactions** 2. Draw the mechanism of formation of the organic products in the reaction shown in **Figure 10**. - **Diagram Description:** - A molecular structure featuring an SH group at position 1 and Cl at position 7. - The reaction proceeds to form two products: one major product (75%) and one minor product (25%) along with HCl. - The major product features a five-membered ring with a sulfur atom, while the minor product also contains a five-membered ring with an additional substituent. - **Figure 10: Mechanism**
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 2 steps with 2 images

SEE SOLUTIONCheck out a sample Q&A here
Blurred answer
Knowledge Booster
Alkynes
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Recommended textbooks for you
Chemistry
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY
SEE MORE TEXTBOOKS