Answered: If no ester was available, could you…

If no ester was available, could you use another carbonyl compound like CH3CH2COOH to perform the reaction? Explain why/why not

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter15: Benzene And Aromaticity

Section15.SE: Something Extra

Problem 13VC: Give IUPAC names for the following substances (red = O, blue = N):

See similar textbooks

Related questions

Q: You lab partner mis-read the lab procedure. Instead of mixing 2-naphthol and sodium hydroxide prior…

Q: Show the product of the following reaction. nucleophilic carbene catalyst

A: The terminal alkenes present at C-13 and C-1 on the same molecule, leading to an intramolecular…

Q: Your research advisor gave you this sequence of two reactions to complete in lab this week. However…

A: The nucleophilic substitution of the hydroxyl (OH) by Chlorine is not possible using HCl. Instead, a…

Q: Using acetylene as your only source of carbon atoms, design a synthesis of pentanal, a 5 carbon…

A: Pentanal is the organic compound is an alkyl aldehyde, chemical formula C₅H₁₀O. It is used in…

Q: Based on the procedure given below, answer the following questions about the aldol condensation…

A: Given that

Q: Show the product of treating this anhydride with reagent

A: Given: Treatment of given anhydride with methanol

Q: Reduction of 2-Methylcyclohexanone Background In this experiment, 2-methyleyclohexanone will be…

A: Given reaction:

Q: Background In this experiment, 2-methylcyclohexanone will be reduced to 2-methylcyclohexanol using…

A: Reduction by NaBH4 gives borane complex derivative with three molecule of reactant after that…

Q: Show the reaction mechanism for obtaining benzamide from benzoyl chloride.

A: the reaction mechanism for obtaining benzamide from benzoyl chloride is shown below

Q: Using curved fishhook arrows, propose a mechanism for the formation of cyclone tame ring of…

Q: Construct a multistep synthetic route from ethylbenzene to (2-bromoethyl)benzene by dragging the…

A: Here, we have to construct a multistep synthetic route from ethylbenzene to (2-bromoethyl)benzene.…

Q: Question attached

A: The chemical reaction in which two substituents are eliminated from the substrate molecules to form…

Q: Aqueous hydrochloric acid was used after the sodium bicarbonate and sodium hydroxide extractions in…

A: The given extraction of organic compounds- Carboxylic acid, Phenol, amine and ketone is carried out…

Q: Draw the reaction scheme for the two reagents shown below that will generate 4-Hydroxyphthalic acid…

A: The Diels-Alder reactions are concerted mechanisms in which the reactants are a substituted alkene…

Q: Write the mechanism for the acid catalyzed dehydration of 1-methyl cyclohexanol. Would you expect…

A: The reaction given is acid catalysed dehydration of 1-methyl cyclohexanol.

Q: Show the product of treating this anhydride with reagent

A: In the organic conversion, suitable reagent converts the reactant into products. Reagents attacks…

Q: Synthesis of Diphenylacetylene This synthesis requires two reactions. The first results in the…

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

Q: Complete the following retrosynthetic analysis (the final product is shown first, and the initial…

Q: In a mixed aldol condensation with unknown aldehydes and ketones experiment, some aldol condensation…

A: An aldol reaction is a carbon-carbon bond formation reaction. The product formed by the aldol…

Q: b) You wanted to produce 2-nitrobenzene-1,4-dicarboxylic acid. For that purpose, you started the…

A: We can solve this question by considering the directing nature of the substituents it means that in…

Q: 2. Based on the type of functional group present in the fabric and the structure of methyl orange,…

A: AZO dyes are organic compound with R-N=N-R' group and long chain of conjugation.They exist as…

Q: Perform the following syntheses. Use the retrosynthetic analysis shown in the example. Be certain to…

A: Predicting and synthesizing the reactants required for the reaction to occur from the known product…

Q: How is ti that the salt KHSO4 is able to act as an acid catalyst for the dehydration of cyclohexanol…

A: Dehydration is a chemical reaction which involves the elimination of water.

Q: Starting with phthalamide (below), provide a step-by-step synthesis of the amine shown below. You…

A: Formation of primary amine by Gabriel pthalamide synthesis. PCC oxidize alcohol to ketone. And…

Q: Background The goal of this experiment was to synthesize benzoic acid using a Grignard reagent…

A: Two questions based on Grignard reaction, which are to be accomplished.

Q: Show the organic product formed when methyl propanoate is reacted with lithium sopropyl amide, then…

A: Lithium diisopropyl amide is a very strong base due to presence of negative charge on nitrogen atom.…

Q: In this part, you will assume that your unknown and the second compound are both dissolved in…

Q: In this experiment we will perform a Grignard addition to an ester. First we will form the Grignard…

A: Grignard reagent plays a vital role in organic chemistry.It has the tendency to form carbon-carbon…

Q: HO OH OH OH NH3 (aq)

A: We have to give the possible mechanism of the given transformation.

Q: Usually the aqueous layer is extracted multiple times with organic. This is more common during a…

A: Extraction is the first stage of purification after a reaction ends. It involves the removal of…

Q: Show the reaction mechanism of 2-butanone with the appropriate reagents to obtain an enamine.

Q: While your aldol reaction was running, your TA announced that the the sodium hydroxide solution…

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…

Q: The compound shown below is the product of a Claisen condensation. Draw structural formulas for the…

A: Given product,

Q: Tertiary alcohols with two identical alkyl groups attached to the alcohol carbon can be made either…

Q: Show the product of treating this anhydride with reagent

Q: General procedure A mixture of 4-hydroxycoumarin (1 mmol), aromatic aldehyde (1 mmol), methyl…

Q: NH2

A: Retrosynthetic analysis is an analysis technique try to solve the problem for the synthesis of…

Q: Show a mechanism for the sulfonation of t-butylbenzene

Q: Show the mechanism of the nucleophilic addition reaction of an alcohol with an isocyanate to yield a…

Q: Show two different ways you would make 2-methyl-3-hexanol via a Grignard reagent, beginning each…

A: Given :- Alkyl halide + organic/inorganic reagents → 2-methyl-3-hexanol To determine :- Two…

Q: In this experiment, we used DCM, Benzoic Acid and NaOH In what form is the organic acid after it is…

A: The reaction between benzoic acid and NaOH cannot just proceed in dry DCM. It needs some amount of…

Q: Show how you would syntheses 3-methoxybenzoic acid from 3-hydroxybromobenzene

A: 3-hydroxybromobenzene is treated with methanol, Williamson's synthesis takes place and a methoxy…

Q: Write down the reaction and mechanism for the experiment.

A: Reaction and mechanism given below.

Q: At the start of lab, Anthony adds vanillin to his Erlenmeyer flask, then adds sodium hydroxide, and…

A: According to the question we have a situation in a lab where an analyst ( Antony) transfers the…

Q: Give a reason why the reduction reaction (with H Pt) of nitrobenzene to aniline is so important.…

A: Nitrobenzene is reduced to aniline by Sn and concentrated HCl. This reaction is called nitrobenzene…

Q: b. (Requires more than 1 step!) Hints: requires more than 1 step; you may use any other reagents…

A: Given product,

Question

In this experiment we will perform a Grignard addition to an ester. First we will form the Grignard reagent from magnesium and bromobenzene and then we will add it to methyl benzoate to produce triphenylcarbinol (also called triphenylmethanol). The sequence and mechanism are attached below.

If no ester was available, could you use another carbonyl compound like CH3CH2COOH to perform the reaction? Explain why/why not

Br
MgBr
THF
+
Mg
warm
phenylmagnesium bromide
bromobenzene
OMgBr
MgBr
HC1
OCH3
+ MgBr(ОH)
+
H2O
methyl benzoate
Triphenylcarbinol

Expert Solution

Step 1

Given is reaction of Grignard reagent.

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

Protection of Groups in Organic Synthesis

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

q D eq eq M req M Preq 0 Match each structural formula on the left to a general functional group classification on the right. CH₂CH₂CH₂CNHCH₂- CH3CH₂CH₂C-OH 0 CH₂CH₂CHCOCH3 CH₂CH3 consomsphẩm CH3 anonpudolg COCCHCH₂CH₂ [Review Topics] CH₂CH₂ CH₂CH3 carboxylic acid ester Clear All anhydride amide [References] none of the above Previous Nex Save
PhCO₂H + OCH3 O benzene O PHOCH3 O PhCO2 O PhCO2CH3 X?
Provide reactants, reagents, and/or products for the followin NH2 + H
H3C-N 'N CH3 CH3 N N lol H3C Hofer CH3 N,N-Dimethyloxamide
Which compound/structure has an incorrect common name given below it? CO- Na+ sodium benzenylate CH3CH2ČOH propanoic acid CH;=CHCNH, propenamide CH;OCH methyl methanoate CH3CI ethanoyl chloride
Above all, nomenclature-wise, the following compound is a(an) aldehyde alkene ketone aromatic conjugated aromatic ہے
Predict the IUPAC Product name. (Hint: first sketch the product then name choosing the correct IUPAC PRODUCT NAME BELOW). H, Pt O 1-pentanone O 1-hydroxypentane 1-hydroxypenten-1-ol 2-hydroxypenten-2-al O 1-hydroxypentanol O 2-hydroxypenten-2-ol
Citronellol ((3R)-3,7-dimethyloct-6-en-1-ol, C10H20O) is an organic fragrance found in the oil extracted from lemon grass. a) Name the two functional groups present in the molecule. b) When a few drops of bromine dissolved in hexane is added to a sample of citronellol the brown colour of the bromine rapidly disappears. i. What type of chemical reaction has occurred? ii. Draw the structure of the product formed. iii. Name the product. c) The product formed when citronellol is heated with a mixture of potassium dichromate and sulfuric acid gives a yellow/orange precipitate when shaken with Brady’s reagent (2,4-dinitrophenylhydrazine). It also shows a positive result with Fehling’s solution. i. What type of chemical reaction has occurred ? ii. What type of functional group is present in the product? d) Explain the type of stereoisomerism which may occur in citronellol.
C10T05Q3420 Give the major organic product for the following reaction. H H H catalytic heat if There is no reaction under these conditions or the correct product is not listed here.
Give IUPAC names for the following substances (red = O, blue = N):
9. Draw the structural formulas for the product(s) of each of the reactions below. ("n" indicates "many".) | b) n cIC(CH2)6CCI + n HO(CH2)2OH → |
Provide only a single name (systematic, derived, or common) for the following compound.