Please with the information provided how do I draw a balanced equation for the reactions by using acetic anhydride as the acylating agent and dicholomethane as the reaction solvent. of the 7-bonds of benzene toring and regenerate the catalyst (step 3). When the acyl group is acetyl (CH3as the acylating agent rather than acetyl chloride. The anhydride is safer to work with and it usually provbetter yields and a simpler work-up. More catalyst is needed with acetic anhydride however, because somthe aluminum chloride complexes with the acetic acid produced during the reaction, making it ineffectivecatalyst. As a rule, 2-3 moles of AlCl3 are used per mole of acetic anhydride.Step 1Step 2Step 3RH+CIR+AICI 3RRacylium ionR++ H+AICI4arenium ionAICI4Figure EAS.2: Mechanism of Friedel-Crafts acylationRAICI3 + HCI Friedel-Crafts Acylation ReactionDraw a balanced equation for the reaction. Include drawings of the structures of the reactant and all threepossible methoxyacetophenone isomers.

We know, Friedel Crafts Acylation reaction is an Electrophilic Aromatic Substitution Reaction. Here,…

Answered: Please with the information provided…

Please with the information provided how do I draw a balanced equation for the reactions by using acetic anhydride as the acylating agent and dicholomethane as the reaction solvent.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter17: Alcohols And Phenols

Section17.SE: Something Extra

Problem 77AP

See similar textbooks

Related questions

Q: Write chemical equations expressing each of the following: (a) Preparation of o-nitrophenyl acetate…

A: “Since there are multiple questions and it is not mentioned that which one has to be solved so I am…

Q: Draw a structural formula for the product formed by treating butanal with reagent. Q.) LiAlH4…

A: The given reactant is butanal.

Q: Compare and explain the acidity of phenol, ethanol, acetic acid. (Using pKa, structures of conjugate…

A: the acidity of phenol, ethanol, acetic acid can be explain on the basic of there respective…

Q: Provide the name of the product after heptanoyl chloride reacts with propan-1-ol under acidic…

Q: Please provide a balanced chemical equation for the following reactions: 2-naphthol + NaOH…

A: 2-Naphthol has the following structure:

Q: 8) Write the condensed structural formula of the ester formed when each of the following react with…

A: In acid medium carboxylic acid and alcohol react and produce ester.

Q: N,N- Dimethyl aniline reacts with Diazotized Sulfanilic acid to form Methyl Orange

Q: (a) 3-Methyl-2-pentanone is condensed with acetophenone in alkaline medium an

A: Since, you have asked multiple question, we will solve the first question for you. If you want any…

Q: Using chemical structures draw the complete chemical reaction of Acetone with benzaldehyde under…

Q: draw the reaction scheme of Benzoic acid,ethanol,benzene and additive of NaOH to produce ethyl…

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

Q: Why is terbutyl chloride the organic phase and hydrochloric acid is the aqueous phase in the…

Q: Starting with the structure of phenol, draw resonance structures that show how a hydroxyl group is…

A: The hydroxyl group (-OH) in phenol is an electron-donating group due to resonance. Resonance…

Q: Which of the following reducing agents is used in a reductive amination? You may choose more than…

A: An organic conversion is a process of converting one organic chemical to another organic compound…

Q: Provide the name of the product after heptanoyl chloride reacts with propan-1-ol under acidic…

A: The product of reaction between heptanoyl chloride and propanol can be predicted by its mechanism

Q: Describe a procedure to synthesize the ester ethyl ethanoate, starting from…

A: Ethene upon hydration in presence of acidic medium gives ethanol Ethanol further oxidised into…

Concept explainers

Aldehydes and Ketones

Aldehydes and ketones are organic compounds that have a carbonyl group, C = O, as their functional group. They both differ in the placement of this carbonyl group in their structures.

Question

Please with the information provided how do I draw a balanced equation for the reactions by using acetic anhydride as the acylating agent and dicholomethane as the reaction solvent.

of the 7-bonds of benzene to
ring and regenerate the catalyst (step 3). When the acyl group is acetyl (CH3
as the acylating agent rather than acetyl chloride. The anhydride is safer to work with and it usually prov
better yields and a simpler work-up. More catalyst is needed with acetic anhydride however, because som
the aluminum chloride complexes with the acetic acid produced during the reaction, making it ineffective
catalyst. As a rule, 2-3 moles of AlCl3 are used per mole of acetic anhydride.
Step 1
Step 2
Step 3
R
H
+
CI
R
+
AICI 3
R
R
acylium ion
R
+
+ H+
AICI4
arenium ion
AICI4
Figure EAS.2: Mechanism of Friedel-Crafts acylation
R
AICI3 + HCI

Friedel-Crafts Acylation Reaction
Draw a balanced equation for the reaction. Include drawings of the structures of the reactant and all three
possible methoxyacetophenone isomers.

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

Trending now

This is a popular solution!

Step by step

Solved in 4 steps with 3 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

Fill in the missing reagents a-e in the following scheme:
Draw all the bonds out fully mastering wont accept N(CH3)2
Which is the best reaction sequence to synthesize m-bromobenzenesulfonic acid from benzene? Br ex OH 1) CH3CI, AIC13, 2) Br2, AlBr3 1) ethene, HF, 2) Br2, FeBr3 1) Br2, FeBr3, 2) H2504 1) Br2, FeBr3, 2) CH3COCI, AICI3 1) H2SO4, heat 2) Br2, FeBr3
Step 4: In an acid-catalyzed epoxide ring opening, the epoxide is first protonated and can then be attacked by weak nucleophiles. H HO: :Nuc Nuc Weak nucleophiles such as water and alcohols can react with the protonated epoxide. One of the main differences between base-catalyzed and acid-catalyzed epoxide ring openings is the regiochemical product expected. In an acid-catalyzed reaction, if one of the epoxide carbons is tertiary and the other primary, the nucleophile will attack at the more substituted carbon. If the epoxide is monosubstituted, the nucleophile will attack preferentially at the primary carbon vs. the secondary carbon. Which reaction will not give the indicated product? N 1. CH,CH,O 2. H₂O OH CH₂CH₂OH, H* N CH₂CH₂OH, H 1 CHICH,O 2. H₂O HO HO H- H
help please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all working
please answer in text form and in proper format answer with must explanation , calculation for each part and steps clearly
what is the forward reaction follwing the arrow whilst stating the reagents by doing retrosynthetic analysis of the final product
Show the organic product formed when methyl propanoate is reacted with lithium diisopropyl amide, then methyl butanoate is slowly added to the mixture. The mixture is neutralized with aqueous acid to obtain a neutral product. Show the steps in the mechanism as reactant is converted to final product. show appropriate arrow pushing and any charges, and draw a box around the final product.
From benzene, organic compounds with 6 carbons of less and any other inorganic compund you want. Synthesize the following naphthalene derivative.
starting with ethyl acetoacetate and formaldehyde as your only source of carbons synthesize the following
1) LiAlH4; ) H3O+ will do which of the following reactions? 3-Phenyl-butanoic acid → 3-phenyl-butan-1-ol Benzene → cyclohexane Benzoic acid → benzaldehyde 2-Phenyl-hexanoic acid → benzoic acid and carbon dioxide 2,3-dimethyl-pent-1-yne → 2,3-dimethyl-pent-1-ene
Draw the MAJOR organic product(s) for each of the following reactions/sequence of reactions. OEt ΕΙΟ OEt OH 1) PCl3 / Br₂ NH2 2) / pyridine 1) EtONa / EtOH 2) H3O+ (dilute) 1) EtONa / EtOH 2) Ph 3) NaOH / H₂O Br 4) H2SO4/H₂O/heat OH 1) SOCI₂ 2) HO- / Et₂N NO2 1) MCPBA / CF3SO₂H 2) Ph-NH2/pyridine 1