Draw the structure of the aldehyde or ketone and the Grignard reagent that will react to form the following compound:CH3You do not have to consider stereochemistry.In cases where there is more than one answer, just give one.• Draw the Grignard reagent as a covalent magnesium bromide.Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.Separate multiple reactants using the + sign from the drop-down menu.CPopy asteChemDoodle

Grignard reagent is formed when magnesium reacts with an alkyl or aryl halide. Chemical formula for…

Answered: Draw the structure of the aldehyde or…

Draw the structure of the aldehyde or ketone and the Grignard reagent that will react to form the following compound: CH3 -O-

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter25: Enolate & Enol Nucleophiles

Section: Chapter Questions

Problem 11CTQ

See similar textbooks

Related questions

Q: Draw the structure of the acyclic polyhydroxy aldehyde that cyclizes toattached hemiacetal.

A: Carbohydrates are the component of food. They are also called sugars. Aldohexoses are the…

Q: [References] Draw the reactant you would use to make the epoxide shown using a Sharpless epoxidation…

A: Sharpless assymetric epoxidation is used for allylic alchohol . when -DET is used the epoxide forms…

Q: Write down the reaction of acetaldehyde with the following. (a) Tollens' reagent (b)…

A: Tollen's reagent is ammoniacal silver nitrate. It is an oxidising agent which oxidises aromatic and…

Q: ? H3C a) OH ОН H3C OCH2CH3

A: Reacting the reactant with ethyl bromide in presence of NaOH will produce the final product. The…

Q: (a) Tollens' reagent

A: the first part is answered as per rules

Q: How can you drive the equilibrium toward the formation of the acetal in the addition of alcohol to a…

A: As per our guidelines , we can only solve first question. Please resubmit other questionas next…

Q: Draw the product of the following reaction. CO2CH2CH3 1. 2 eq. CH3CH2M9BR 2. H3O* • Draw only the…

A: In this question, reagent and starting material are given and you will findout the Product of the…

Q: Draw the organic product that forms when the following compound is treated with aqueous NaOH. он CH3…

A: NaOH is base so it abstracts proton.

Q: Draw the major products formed in the following reaction involving an acid anhydride dissolved in…

A: The reaction of an acid anhydride with an alcohol gives ester and a carboxylic acid as the products.…

Q: Draw the structure of the major product formed in the following reaction when the aromatic aldehyde…

A: The methoxide ion acts as a base and deprotonates the methyl acetate to form the enolate ion. The…

Q: Which one of the following carbonyl compounds does not form an alcohol when it reacts with a…

A: We will draw the products with each reactant and answer the question.

Q: Reaction 1 1.03 2. DMS Reaction 2 1. BH3 2. NaOH,H₂O₂, H₂O KMnO 1. BH3 2. NaOH H₂O

Q: The following alcohol can be prepared via reduction of a ketone or aldehyde. Draw the aldehyde or…

A: Solution Aldehydes and ketones square measure most promptly reduced with binary compound reagentsThe…

Q: Draw the reactant you would use to make the epoxide shown using a Sharpless epoxidation with t-BUOOH…

Q: What aldehyde or ketone would be obtained when the following compound is heated in a basic aqueous…

A: The given product 2,4 -dicyclohexyl- 3 -hydroxybutanal of an aldol addition is heated with hydroxide…

Q: H -СН+ 2СHCH-ОН

Q: Draw the structure of the major product formed in the given reaction when the aromatic aldehyde is…

A: The methoxide ion acts as a base and deprotonates the methyl acetate to form the enolate ion.

Q: Draw reaction of carbonyl compounds with an acetylide ion forms an a-hydroxy alkyne.

A: Acetylide ion acts as a nucleophile and the nucleophilic addition reaction takes place at the carbon…

Q: Draw the structure of each molecule. (a) 2,2-dimethylpropyl hex-3-ynoate; (b) cyanoethanoic…

A: (a) The structure for IUPAC name 2, 2-Dimethylpropyl hex-3-ynoate is:

Q: Draw the structure of the acyclic polyhydroxy aldehyde that cyclizes toattached hemiacetal.

Q: Click the "draw structure" button to launch the drawing utility. Draw the product formed when the…

A: Aldol condensation It is a condensation reaction where enolate ion reacts with a carbonyl to give…

Q: Which Grignard reagent, followed by aqueous workup, can be used to convert acetone into…

Q: What two β-keto esters are formed in the Dieckmann reaction of the following diester?

A: Dieckmann Reaction: This reaction is for formation of by β-keto esters from diesters with base.…

Q: 10. Which one of the following compounds is an acetal? || CH3C-H OEt a) CH3COCH3 b) d) HO OEt

A: Carbonyl compound (aldehyde and ketone) reacts with an alcohol to form hemiacetal in the presence of…

Q: Write down the reaction of acetaldehyde with the following. (a) Tollens' reagent (b)…

A: (a) Tollens test (b) 2,4 -DNP test (c) Iodoform test

Q: The following compound is prepared by Fischer esterification of which combination of reagents? COCH3…

A: Fischer reaction is the reaction between carboxylic acid and alcohol in the presence of acid and…

Q: When a 1:1 mixture of ethyl propanoate and ethyl butanoate is treated with sodium ethoxide, four…

A: Claisen condensation occurs between two esters in the presence of base and form β-keto ester. It is…

Q: Draw the product formed when the following a.ß-unsaturated ketone is treated with [1] (CH,=CH),CuLi;…

Q: Which of the following thiols will produce this disulfide after oxidation?…

Q: 1) Draw AND name the product that would result upon treatment of R-3-methylheptanal with Excess…

A: We’ll answer the first question since the exact one wasn’t specified. Please submit a new question…

Q: The following alcohol can be prepared via reduction of a ketone or aldehyde. Draw the aldehyde or…

A: To draw the aldehyde or ketone that would be required in the preparation of the below alcohol.

Q: When a 1:1 mixture of acetone and 2-butanone is treated with base, six aldol products are possible.…

A: Each pair should have two isomers so totally six products in the below the scheme have chiral…

Q: Draw the structure of the aldehyde or ketone and the Grignard reagent that will react to form the…

A: When 3-methylpentanal reacted with Gridnard reagent (HMgBr) followed by acid hydrolysis to form…

Q: Draw the structure of the acyclic polyhydroxy aldehyde that cyclizes to each hemiacetal

A: First structure-

Q: Draw the organic product that forms when the following compound is treated with aqueous NaOH. он +…

A: Note: Alcohols react with sodium hydroxide give alkoxide ion (Here OH is having acidic proton,…

Q: Draw line structures of the following compounds and the product you would obtain from the reduction…

A: Line structures can be defined as the organic structure of compounds without the indication of…

Q: Draw the organic product that forms when the following compound is treated with aqueous NaOH.

A: In general alcohols are less acidic , hence when they react with Na metal , NaH it gives sodium…

Q: What aldehyde or ketone would be obtained when the following compound is heated in a basic aqueous…

A: The given molecules would undergo retro aldol condensation in which the β-hydroxyaldehyde or…

Q: Draw the structure of the product formed when 2-methylbutanal is treated with cold aqueous base.…

A: Please find below the reaction mechanism taking place.

Q: Show the product expected when the following unsaturated 8-ketoester is treated with each reagent.…

A: The product expected when the given unsaturated δ-ketoester is treated with the given reagent has to…

Q: Draw reaction of an aldehyde or a ketone with excess alcohol forms first a hemiacetal and then an…

A: Aldehydes and ketones reacts with excess alcohols forms hemiacetal which then rearranges to acetal.…

Q: Which ketone in each pair is more reactive? a. 2-heptanone or 4-heptanone b. bromomethyl phenyl…

A: The structure of given pairs is represented as follows:

Q: What two β-keto esters are formed in the Dieckmann reaction of the following diester?

A: Concept introduction- Dieckmann Reaction- This reaction is for formation of by β-keto esters from…

Q: When this compound is combined with a trace amount of sulfuric acid and molecular sieves, which…

Q: Name a reaction in which a acetone reacts with NaOH to give alpha beta unsaturated ketone

Q: Draw the structures of compounds X and Y in the box provided. Ph 1. Dihydroxylation 2. HIO4 OH…

A: In the given reaction, one compound reacts to form two products i.e., compound X and compound Y.…

Q: Draw the structure of the product that is formed when the compound shown below is treated with the…

A: Hydroboration–oxidation reaction: Alkene gives an electrophilic addition reaction with borane.…

Q: Draw reaction of an aldehyde or a ketone with cyanide ion under acidic conditions forms a…

A: Cyanohydrin Formation is a Nucleophilic Addition reaction. Aldehydes and ketones add reversibly to…

Q: Draw the products formed when each ester is treated with lithium hydroxide and water. Reaction A…

Q: The following molecule can be formed via an intramolecular aldol addition reaction. Draw the organic…

A: Aldol condensation is a condensation reaction for an enol or an enolate ion. The final product form…

Concept explainers

Reactions at the Alpha Carbon Atom

The position next to the ketone or aldehyde functional group is termed as alpha position and the reaction which occurs at alpha position is called alpha substitution reaction. In an alpha substitution reaction, the alpha proton atom is substituted by an electrophile by the formation of an enol intermediate or enolate ion intermediate. Most of the carbonyl compounds go through an alpha substitution reaction.

Question

Draw the structure of the aldehyde or ketone and the Grignard reagent that will react to form the following compound:
CH3
You do not have to consider stereochemistry.
In cases where there is more than one answer, just give one.
• Draw the Grignard reagent as a covalent magnesium bromide.
Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
Separate multiple reactants using the + sign from the drop-down menu.
C
P
opy aste
ChemDoodle

Expert Solution

This question has been solved!

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

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Step 3

VIEW

Step by step

Solved in 3 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

Draw eugenol as a line structure. The double bonds of the benzene ring are fairly unreactive unless you use special catalysts. But the double bond on the side group is reactive. Draw the mechanism of eugenol reacting with HBr to form the two possible carbocation intermediates. Put your intermediates into square brackets. Label each carbocation as a methyl carbon or 1°, 2°, or 3°. Then circle a more stable carbocation if one is more stable. Can you guess what the final product is?
(1, 3) Draw the structure(s) of the major organic product(s) of the following reaction. You do not have to consider stereochemistry. If a compound is formed more than once, add another sketcher and draw it again. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu.
C6H5CO2CH2C6H5 can be synthesized by an SN2 reaction. Draw the structures of the alkyl chloride and nucleophile that will give this compound in highest yield. Use the wedge/hash bond tools to indicate stereochemistry where it exists. Include all valence lone pairs in your answer. Separate multiple reactants using the + sign from the drop-down menu. When a metal counterion is needed, use Na+, but draw it in its own sketcher.
The compound shown below is the product of a Claisen condensation. Draw structural formulas for the reactants: ester and enolate ion. Assume all esters to be ethyl esters. Do not include counter-ions, e.g., Na+, I-, in your answer. Draw the enolate ion in its carbanion form. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu.
Draw the organic product(s) of the following reaction. You do not have to consider stereochemistry. Include cationic counter-ions, e.g., Na+ in your answer, but draw them in their own sketcher. If no reaction occurs, draw the organic starting material. Separate multiple products using the + sign from the drop-down menu.
For the 6-carbon molecule below, how would you expect it to break into two pieces? a. two 3-carbon units b. one 2-carbon unit and one 4-carbon unit c. one 1-carbon unit, one 2-carbon unit, and one 3-carbon unit d. one 1-carbon unit and one 5-carbon unit I'm having a hard time identifying the correct location of Beta and Alpha. If the carbonyl beta is the second bond over from carbonyl, then the breakage would occur at bond C3-C4. This would then result in two 3-carbon units, right? The molecule in the image looks like fructose which would result in two 3-carbon units.
In the drawing area below, create an acetal with 1 methoxy group, 1 ethoxy group, and a total of 8 carbon atoms
This question has multiple parts. Work all the parts to get the most points. a Draw all of the monochlorination products that you might obtain from the free-radical chlorination of 2,2,4-trimethylpentane. You do not have to consider stereochemistry. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple products using the + sign from the drop-down menu.
Draw the structure(s) of the major organic product(s) obtained after workup of the following reaction. Use the wedge/hash bond tools to indicate stereochemistry where it exists. If no reaction occurs, draw the organic starting material. Draw structure(s) of product(s) after aqueous workup. Include counter-ions, e.g., Na+, I-, in your submission, but draw them in their own separate sketcher. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
For Fehling's Test not all aldehydes reacts to this test, what are the limitations and does the samples given below reacts to Fehling's Test? Explain a. formaldehyde b. glucose c. benzaldehyde d. acetone
a) Write out the 3-step arrow pushing mechanism showing how 1-pentene is hydrated to make 2-pentanol. b) Draw the other 2 alkenes(don’t forget cis/trans isomers!) that could also be hydrated to make 2-pentanol. Briefly explain why1-pentene is the best choice.
Write out the mechanism for this hydration of an alkene adding curved arrows to show how electrons reorient to make or break bonds or form new lone pairs