**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**

Answered: Image /qna-images/answer/f13236ea-32ef-4692-818a-26bb278535db.jpg

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

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

Related questions

Q: Which chlorination product is formed via the lowest energy transition state in the rate-determining…

Q: Nal OEt NME2 NaHCO3 ?? ?? 10 °C 25 °C ŅME2 PhMgBr ?? ELOH ?? -78 °C → 25 °C 80 °C

A: For 1,2-addition: i) Nucleophile should be strong, ii) Reaction at low temperature. For…

Q: 5. Predict the organic products of the following nucleophilic substitution reactions, all of which…

Q: Provide a detailed mechanism for the formation of C and draw it in the box above. Draw the reaction…

Q: N3 H Predict the product of the following multi-step reactions. The points per question is the…

A: In case of first reaction, presence of base it abstract acidic proton and form carboxylate ion which…

Q: With respect to the mechanism of the base-catalyzed hydrolysis of methyl benzoate (see below) to…

Q: 애 1. TS CIS Py > 2. Mea NH SN-

A: Product of following reaction can be made by applying appropriate reaction mechanism.

Q: Consider the reaction below. What would happen to its rate if the concentration of the the alkyl…

A: The effect of concentration of reactants on the rate of given reaction is to be explained. The given…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. FeBr3 Select to Draw Br Q

A: This is an example of electrophilic substitution reaction of benzene

Q: Which reaction sequence will bring about the following transformation? LMg. THE 2. co, 1. NaOH.DMSO…

A: In organic transformations, appropriate reagent converts the reactants into products. Reagents…

Q: Q3. Q4. :S: CI Br H₂O dilute OH-

A: Question 3:The given question is an example of neighbouring group participation reaction. The sulfur…

Q: can you please help me . been struggling with hw

A: We have given two organic reaction and we have to find product of this reaction.

Q: 8. Provide a complete mechanism for each reaction below, including all curved arrows, reactive…

A: Here we are required to show the mechanism for the formation of the product from the given Starting…

Q: For the SN 1 reaction, draw the major organic product, identify the nucleophile, substrate, and…

A: The question is based on organic reactions. we need to identify the product formed and explain…

Q: Could you draw the full arrow pushing mechanism for each of these and give the proper name for this…

A: The nucleophilic addition-elimination reaction takes place in two steps:Step 1: The nucleophile…

Q: help #1

A: Ozonolysis of alkynes produces ozonide which on treated with acetic acid to form the dicarboxylic…

Q: raw curved arrows to show the movement of electrons in the step of the mechanism shown below.…

A: The curved arrow mechanism is a representation of a reaction in which reactant molecules convert…

Q: What is the nucleophile in the reaction shown? Br 1 e + Na CN || CN ||| + Na Br IV

A: Nucleophilic substitution reaction is a fundamental class of organic reactions in which a leaving…

Q: ile.php/1337784/ T Add text I Draw ID Page view A Read aloud 4. Show the mechanism and draw a…

Q: 1a. Predict the product(s) shown for the set of reactions below and show the full mechanism. u 1.…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Draw the scheme of reaction for the multi-step synthesis shown in figure 1

A: The first step is the N-acylation of p-chloroaniline (2) with maleic anhydride (1) to give the…

Q: k. HN H+ (cat) 1. methyl vinyl ketone N. 1. (Michael) 2. H3O* 3. NaOH (aldol)

Q: Draw the organic product/s formed in each reaction. Then, identify the mechanism for each reaction…

A: A. t-butoxide is a bulky base favors elimination and sn2 product is minor. B. Primary alkyl halide…

Q: EtO ₂C. CO₂ Et Et- -0, A then Ph Br. Ph .CO₂ Et

Q: Can someone show me the complete mechanism with arrows? How would the reaction be different if no…

A: In this question, we will show the complete mechanism with using curved arrows. Here, NaOH excess…

Concept explainers

Alkynes

Alkynes are organic compounds that contain at least one triple bond between carbon-carbon atoms. They are a series of unsaturated compounds with a general molecular formula, CnH2n-2.

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**

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

This is a popular solution!

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 2 steps with 2 images

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

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.

Similar questions

8. Show the mechanism for the nucleophilic aromatic substitution below. NH2 Br NaNH, ZON + NaBr NO2
3. For the chemical reaction below, answer the following questions H3C CH3 CH3 + HBr a. Draw the correct products of the reaction above (next to the reaction arrow) b. Show a complete mechanism for how the reaction above occurs. C. Draw the reaction coordinate diagram for the exergonic (-AG) reaction above. Label the axes.
но, CH, CHO CHO Drag the appropriate labels to their respective targets. Reset Help I equivalent acid catalyst - H;0 ether H,O CH,OH CH,MgBr но OH HO CH, CHO CHO
Propose the major product for each of the following reactions and propose a reaction mechanism for the reactions they present. Dr. explained that he wants reaction products and a reaction mechanism but I don't understand how to do it, I am only in my 1st semester, I hope you can help me.