Provide the synthetic steps needed to complete the conversion of the starting reactants into the final compound shown in the chemical equation below: O=C=O Cu CEN Special Note: The last step involves making the ester, so you need to make the two reactants needed to make an ester using the reagents above. You are given CuCN, which means the nitrile must be directly attached to a ring at some point, this may provide some guidance regarding whether toluene makes the half with the C=O or the benzene ring does.

Provide the synthetic steps needed to complete the conversion of the starting reactants into the final compound shown in the chemical equation below: O=C=O Cu CEN Special Note: The last step involves making the ester, so you need to make the two reactants needed to make an ester using the reagents above. You are given CuCN, which means the nitrile must be directly attached to a ring at some point, this may provide some guidance regarding whether toluene makes the half with the C=O or the benzene ring does.

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: Draw the final product of the reaction given below. OH 1, SOCI₂ 2. CH3NH₂ The name of the functional…

Q: uct of the following reaction? use the letters p = of the new functional group? H+ B HN D

A: Reactant is ketone and secondary amine. Ketone and secondary amine react with each other, there is…

Q: Which of the following statements about the reaction shown is not necessarily true? O'Na you' NaOH…

Q: The following reaction is catalyzed by H₂SO4: CH3COOH + CH3CH₂OH → CH3COOCH₂CH3 + H₂O Which type of…

Q: Draw the two different major organic products of this reaction. Ignore inorganic byproducts. 0 TSOH,…

Q: What sort of reaction is shown below? OH Reduction Acid-Base Esterification Addition Elimination…

A: The reaction between an acid and a base to give salt and water is called neutralization reaction.…

Q: Organic Functional Groups Predicting the reactants or products of acetal hydrolysis Determine the…

A: The objective of the question is to find the structure of the missing organic molecule in the given…

Q: Predict the products when 1-propanol is heated in the presence of H . Include all hydrogen atoms in…

A: Organic product is the product that involves hydrogen and carbon atoms.

Q: Draw the most stable form of the organic products formed in the following reacton of ethyl acetate…

A: This mechanism can be done by Claisen condensation reaction. The machanism and most stable form of…

Q: Draw the organic product you would expect to isolate from the nucleophilic substitution reaction…

A: Given reaction is an example of nucleophilic substitution reaction.The substitution reaction is a…

Q: Questions 14-18. Consider each of the esters below when answering the following questions: CO Et…

A: “Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: Draw the structure of the major organic product(s) of the reaction. H3C 1. 2 CH3MgBr, ether 2. H3O+

Q: Draw the organic product you would expect to isolate from the nucleophilic substitution reaction…

A: Alkyl halide is tertiary thus it follows SN1 mechanism.Alcohol is the nucleophile. Mechanism of…

Q: Observations: Test Tube Carboxylic Acid A acetic acid B acetic acid C acetic acid benzoic acid…

A: An esterification reaction occurs between an alcohol and a carboxylic acid via removal of a water…

Q: Complete the following reaction scheme. Keep in mind that the sequence starts with an alkene or…

Q: b. Which of the following is the structure of acetic anhydride? si OH c. When 4-ethoxyaniline reacts…

A: To solve this problem we have to identify the given compound

Q: What type of synthesis is this an example of? Is this showing the addition of a ketone giving a…

A: Organic reactions are those in which organic reactant react to form organic products.

Q: Draw the organic product you would expect to isolate from the nucleophilic substitution reaction…

A: The nucleophilic substitution reaction in which a carbocation intermediate is involved is considered…

Q: When aniline undergoes addition to an electrophile, the carbocation intermediate has a variety of…

A: In the electrophilic aromatic substitution of benzene derivatives, the substitution of incoming…

Q: O || CH3CH2-C-OH (aq) + NaOH (aq) CH3 CH₂-C-0- Na² (aq) + H₂,0 (1)

A: In an acid base reaction, acid reacts with base to form salt and water .This is called…

Q: This is a reduction reaction. Two hydrogens and two electrons are used to reduce the ketone to an…

A: The chemical compound is regarded as a reducing agent which itself get oxidized and reduces the…

Q: Draw a structure for the organic product(s) of the following reaction. OH SH HS OH

A: The compound and its stereochemistry is HS – S – OH – OH – R - SH Under iodine; thiol group…

Q: Le Chatelier's Principle governs many of the reactions we have seen in Chapters 15 and 16, such as…

A: According to question We have to favour the product side That can be done by using Lechatelier…

Q: CH3 НО ОН CH3 H Cortisol a) NaCN b) H3PO4 85% c) NABH4 .. I sבוווי

A: The question is based on the concept of organic reactions. we have to identify which of the…

Q: aldehydes and ketones 1 Which of the following statements about the reaction of aldehydes and…

A: option (c) is correct . Aldehyde when undergoes oxidation reaction in presence of acidified…

Q: Draw the products of the following reactions.

A: In this question we have to tell the product of the reaction.

Q: + F₂ N catalyst The above reactants would undergo a catalyst esterification incomplete combustion…

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

Q: Consider the following Fischer Esterification shown in Figure 2.3 to answer Question 6 and 7: OH HO,…

A: Introduction: According to Le Chatelier’s principles, if there is a change in concentration,…

Q: 1. Predict the products when cyclohexanol is heated in the presence of H+. Show all hydrogen atoms.…

A: Hey, since there are multiple questions posted, we will answer first question. If you want any…

Q: The reduced form of the coenzyme nicotinamide adenine dinucleotide is abbreviated NADH. In the…

A: The reduced form of the coenzyme nicotinamide adenine dinucleotide is abbreviated NADH. In the…

Q: What is the product of the following reaction? سلام 1. KMnO4, HO', A 2. H

A: If there is at least one H at the Benzylic position then in the presence of KMnO4/OH- the whole…

Q: NH, a)

A: This is a multi step synthesis reaction . Detail mechanistic pathway is given below

Question

100%

Provide the synthetic steps needed to complete the conversion of the starting reactants into the
final compound shown in the chemical equation below:
abo
O=C=O
Cu CEN
Special Note: The last step involves making the ester, so you need to make the two
reactants needed to make an ester using the reagents above. You are given CuCN, which
means the nitrile must be directly attached to a ring at some point, this may provide some
guidance regarding whether toluene makes the half with the C=O or the benzene ring
does.

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

Step 2

Step 3

Step 4

Step 5

Trending now

This is a popular solution!

Step by step

Solved in 5 steps with 4 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

How could one convert an aldehyde to a carboxylic acid? Group of answer choices- Reduce the aldehyde with hydrogen gas (H2) Oxidize the aldehyde using a mild oxidizing agent (such as permanganate). Combust the aldehyde with molecular oxygen. Use any of the above; each one would work OK.
What is the missing reactant in this organic reaction? R + CH3- -OH Δ مكم + H₂O Specifically, in the drawing area below draw the skeletal ("line") structure of R. If there is more than one reasonable answer, you can draw any one of them. If there is no reasonable answer, check the No answer box under the drawing area.
Complete these nucleophilic substitution reactions. In each reaction, show all electron pairs on both the nucleophile and the leaving group.
Draw a reaction showing the reactants (the ester and water) and the products (the alcohol and the carboxylic acid) for each ester below. You can google the structures of the esters. Ester 1 aspirin, Ester 2 benzocaine, Ester 3 gamma-butyrolactone
Use a sheet of paper to answer the following question. Take a picture of your answers and attach to this assignment. Draw the mechanism for the acid-catalyzed reaction of acetic acid (ethanoic acid) with the methanol to yield methyl acetate (methyl ethanoate). O O HCI H3C + CH3OH OH H3C OCH 3 + H₂O
Use the carboxylic acid and alcohol listed below to make an ester using a Fischer esterification. Draw a reaction scheme (like on the top of each page in the manual) to show which starting materials and reagents you would use, and name the product using proper nomenclature. Acetic acid (ethanoic acid) Ethanol
The reaction of a Grignard reagent with a ketone followed by dilute acid gives a(n) O primary alcohol. ester. tertiary alcohol. O secondary alcohol.
4a. Which type of molecule is this? Label the nonpolar and polar regions of this molecule. Label the ester bonds and phosophodiester bonds. H₂C-0-C HC-0-C CH, CH,−N O CH₂ O CH3 4b. What products would you obtain if you performed an hydrolysis reaction? Draw them. O=C O=0
Can you help me part B? Which is the formula of this rule of reaction? I don't know which was the rule of the reaction?
What is the product of the following reaction, where an ESTER functional group is treated with lithium aluminum hydride?
Draw the organic product you would expect to isolate from the nucleophilic substitution reaction between the molecules shown. Note: You do not need to draw any of the side products of the reaction, only the substitution product. □ + HO 1 + X S Click and drag to start drawing a structure.
x ✓5 Br 6 Draw the organic product you would expect to isolate from the nucleophilic substitution reaction between the molecules shown. Note: You do not need to draw any of the side products of the reaction, only the substitution product. Ö + X S 8 C 9 Click and drag to start drawing a structure. 10