Identify the starting reagents needed to make the following compound by mixed aldolcondensation.CH30-K+PhA Acetophenone and butanalB Benzaldehyde and pentan-2-oneC Acetophenone and butan-2-oneD Benzaldehyde and pentan-3-one

In aldol condensation reaction an enol or an enolate ion reacts with a carbonyl compound to form a…

Identify the starting reagents needed to make the following compound by mixed aldol condensation. CH3O-K+ Ph A Acetophenone and butanal B Benzaldehyde and pentan-2-one C Acetophenone and butan-2-one D Benzaldehyde and pentan-3-one

Identify the starting reagents needed to make the following compound by mixed aldol condensation. CH3O-K+ Ph A Acetophenone and butanal B Benzaldehyde and pentan-2-one C Acetophenone and butan-2-one D Benzaldehyde and pentan-3-one

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter17: Alcohols And Phenols

Section17.SE: Something Extra

Problem 47AP

See similar textbooks

Related questions

Q: Which of the following is the aldol addition product of two butanal molecules 2 CH3CH₂CH₂CH NaOH,…

A: Aldol condensation is a type of organic reaction that involves the condensation of two molecules of…

Q: H₂C H3C. AXE OCH 3 CH3 H3CO Aldehydes and ketones react reversibly with two equivalents of alcohol…

A: To draw the arrow for the iven step of mechanism

Q: Which reagent would you use to accomplish each of the following transformations? Options (please…

A: Reagent 1: NaOEt Reagent 2: BH3-H2O2 Explanation:Step 1: Reaction Step 2: MechansimStep 1 is…

Q: Name the following compound. CI O O O Br 2-bromo-4-chloro-6-oxyoxane 6-bromo-4-chloro-2-oxyoxane…

A: Here an organic compound is given and we have to find out the correct name of the given compound.

Q: Draw the hemiacetal that is formed when the ketone is treated with one equivalent of methanol…

Q: Of the following compounds, which one will form a silver mirror upon treatment of Tollen's reagent?…

Q: 3. Complete the following synthesis using any reagents of your choice: Me Me COOH

Q: What are the products of the following reaction? H O OCCH, H CH₂ Multiple Choice…

A: Given that, the reaction is:

Q: 4) The following enone, 3-methylcyclopent-2-enone, was prepared through an intramolecular aldol…

Q: H روه Base Aldol Product the Mal NaOH H₂0 Condensation Product

A: Organic reactions are those in which organic reactant react to form organic products. In the given…

Q: Choose the best reagents to complete the following reaction. :(CH2OH)2, TSOH OH OH Q Q A NaOH B H2O…

A: Reaction:Reagent: Need to be determine

Q: An aldol addition can be catalyzed by acids as well as by bases. Propose a mechanism for the…

A: Aldol addition reaction: In this reaction two molecules of carbonyl compounds like aldehyde or…

Q: Br ácido acético 25°C CI CH3SNA DMSO CH3 CH3CH2ONA etanol *Br calor

A: The given reaction is shown below:

Q: What product is formed from the addition of NaOH to p-tertbutylphenol? Group of answer choices a…

A: The reactants given are 1) Acidic compound i.e p-tertbutylphenol. 2) Basic compound i.e NaOH.

Q: Rank the following esters in order of decreasing reactivity in the first slow step of a nucleophilic…

A: For the formation of the tetrahedral intermediate, the nucleophilic acyl substitution reaction takes…

Q: Identify the best reagents to complete the following reaction. OH

Q: a CH3-CH-CH2-CH2-CH3 OH b CH2-CH2-CH2-CНз Но

Q: The compound having the HIIGHEST percentage of cyclic hemiacetal at equilibrium is Compound The…

Q: 5. Propose a mechanism for the base-catalyzed hydrolysis of the nitrile. -CEN H₂O NaOH 6. Propose a…

A: 1) base catalysed hydrolysis of nitrile concerted nitro group to carboxylic acid

Q: горanol горanol anol panoic acid ropanone

A: In this reaction reactant is an ester and this is ester hydrolysis. The hydrolysis of ester will…

Q: Using sodium borohydride to reduce a ketone leads to which of the following? 1° alcohol 2º alcohol…

A: Due to comparative soft nature of Sodiumborohydride it only reduces aldehyde and ketone to alcohol .…

Q: Step 3: If excess alcohol is present in the hemiacetal, the hemiacetal can be further converted to…

A: Hemiactal group contains carbon atom connected with one OR group and one OH group. Acetal group…

Q: In an aldol condensation reaction, acetone and benzaldehyde are mixed in the presence of sodium…

A: Given: In an aldol condensation reaction, acetone and benzaldehyde are mixed in the presence of…

Q: How to synthesise 1-cyclohexylcyclohexanol from cyclohexanone?

Concept explainers

Aromatic Compounds

Aromatic organic compound or aromatic system is an important class of hydrocarbons under the branch of organic chemistry. Aromatic compounds are also called arenas. The definition of aromatic organic compounds can be stated as a class of organic compounds with a planar cyclic ring of atoms bonded through alternated single and double bonds. Due to these alternating bonds, a peculiar feature termed as ‘resonance’, that is, delocalization of pi electrons or the electrons is shared within the atoms of the ring which are present in the aromatic compounds. The word ‘aromatic’ includes a Greek word ‘aroma’ which means smell, indicating that they were named as such due to the sweet odor they produce. Many well-known flavors such as vanilla, cinnamon, and few scents from flowers are extracted from aromatic compounds. Benzene with chemical formula C6H6 is a very common aromatic compound that contains six atoms of carbon held in the cyclic ring of alternate double bonds. It is also to be noted that not all aromatic compounds contain benzene ring. This can be explained by Huckel’s rule.

Question

Identify the starting reagents needed to make the following compound by mixed aldol
condensation.
CH30-K+
Ph
A Acetophenone and butanal
B Benzaldehyde and pentan-2-one
C Acetophenone and butan-2-one
D Benzaldehyde and pentan-3-one

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 1 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

Using your reaction roadmap as a guide, show how to convert 1-propanol into 2-hexyne. You must use 1-propanol as the source of all carbon atoms in the target molecule. Show all reagents needed and all molecules synthesized along the way.
How would you carry out the following reactions? More than one step may be required. (a) 3-Hexyne â†’ 3-Hexanone (b) Benzene â†’ m-Bromoacetophenone (c) Bromobenzene â†’ Acetophenone (d) l-Methylcyclohexene â†’ 2-Methylcyclohexanone
Using your reaction roadmap as a guide, show how to convert cyclohexanol into racemic trans-1,2-cydohexanediol. Show all required reagents and all molecules synthesized along the way.
What product is formed from the addition of NaOH to p-tertbutylphenol? Group of answer choices a compound with addition of an OH group to p-tertbutyl phenol the sodium salt of p-tertbutylphenol, sodium p-tertbutylphenoxide a protonated version of p-tertbutylphenol there is no reaction
What is the major product of the following reaction? OH NO₂ FeBr B12 1-bromo-2-nitrobenzene 2-hydroxyaniline 2-bromo-6-nitrophenol and 4-bromo-2-nitrophenol O 3-bromo-2-nitrophenol and 5-bromo-2-nitrophenol
Choose the correct product for the following reaction 4-methylcyclohexanone + Br2/H3O+ --> product? A 2,6-dibromo-4-methylcyclohexanol B 1-bromo-4-methylcyclohexanol C 2,6-dibromo-4-methylcyclohexanone D 2-bromo-4-methylcyclohexanol E 2-bromo-4-methylcyclohexanone
Which reagent would you use to accomplish each of the following transformations? Options (please type exactly as shown and chose the most relevant reagent): B2H6 Et2O H2O-H2SO4 t-BuONa BH3-H2O2 EtOH B(OH)3-NaOH B(OH)3-H2O NaOEt Reagent 1: Reagent 2:
Select all the syntheses that produce the pictured ether in better than 50% yield: 2-butanol treated with sodium hydride followed by methyl chloride a 50/50 mixture of methanol and 2-butanol heated with concentrated sulfuric acid methanol treated with sodium hydride followed by 2-chlorobutane O 2-butanol treated with sodium hydride followed by chloroethane
What are the products obtained from saponification of isopropyl benzoate with sodium hydroxide? O Sodium propanoate + phenol O benzoic acid + 2-propanol O 2-Propanoic acid + benzyl acohol O Sodium benzoate + 1-propanol O Sodium benzoate + 2-propanol
How would you use Grignard reagent on an aldehyde or ketone to synthesis the following compounds?
Does this have the ability to form a hemiacetal or acetal if methanol is added in the presence of heat and acid? Draw the product.
What is the reaction mechansim for the following reaction?