Explain Carboxylation of methoxy benzene? What are the best sets of reagents. Define in details ?

Q: Which one of the molecules shown below prefers to exist as its enol tautomer?

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Q: Predict the oxidation product of treating the given alkene with a peroxyacid reagent. Omit…

A: The given reagent is per acetic acid PAA. This reagent can oxidize high electron rich centers.

Q: What is the major organic product obtained from the following reaction? B

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Q: Q1. Outline two methods of phenols synthesis. Q2. Give a concise account on the nomenclature of…

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Q: the

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Q: Provide the curved-arrow mechanism to account for the following nucleophilic addition- elimination…

A: Nucleophile attacks on carbonyl carbon to produce tetrahedral intermediate. This tetrahedral…

Q: Synthesize from benzene. (Hint: All of these require diazonium ions.) ) 3-n-propylphenol

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Q: Complete the following reactions, clearly indicating regio-and stereochemistry where applicable. In…

A: Reaction is given below.

Q: Explain how Hammond's postulate accounts for the higher selectivity of bromination reactions as…

A: We have to explain how the Hammond postulate accounts for the higher selectivity of bromination…

Q: pyridine reacts with 1-bromobutane to give?

A: When alkyl halide reacts with pyridine, lone pair electrons of N attacks the alkyl group &…

Q: Draw and name structures of all products expected from monobromination of the following and indicate…

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Q: To make Halocyclopentane, what reagents and substartes are needed? Which one(below) is related with…

A: Alkyl halides (also known as haloalkanes) are compounds in which one or more hydrogen atoms in an…

Q: Give the major products or reagents represents in the following reactions:

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Q: NaN N'

A: Nucleophilic addition- elimination reaction is a reaction in which the substitution of any group…

Q: Provide Examples of dehydrohalogenation of dihalides to afford alkynes ?

A: Alkynes- Unsaturated hydrocarbon containing carbon carbon triple bond is known as alkyne. Alkynes…

Q: Explain the steps involve in the below organic reaction in detail ONa H3N

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Q: What is more stable acetate (CH3COO-) or ethoxide (CH3CH2O-)? In three words or less explain your…

A: Stability of anion: Primary carbanion is more stable than secondary and tertiary carbanions due to…

Q: Provide another method for preparation of cyclohexene from another compound except cyclohexanol

A: Applying concept of elimination reaction for formation of cyclohexene.

Q: Provide the appropriate reagents or product in the following examples.

A: Given ; reactant

Q: Provide efficient syntheses of the following compounds using 1-pentene as your starting material and…

A: Reaction scheme is usually framed by mainly considering the factors like atom economy, availability,…

Q: ОН

A: These reactions are generally proceeds in a heating or light conditions.  Here we are given with…

Q: The transformation takes place via two sequential pericyclic reactions. Identify the two reactions…

A: Given & To find:-

Q: Illustrate the mechanism of forming alkynes from a 1,2-dihalide and a vinyli halide. Show…

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Q: Give the major organic product(s) for the following reaction:

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Q: What is the major product formed, when toluene undergoes Friedel-Craft's alkylation with vinyl…

A: Friedel-Crafts Alkylation reaction is the reaction of toulene with haloalkanes in presence of…

Q: Why do both the following alkenes yield the same product upon reaction with hydrobromic acid?…

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Q: Explain the steps involve in the below organic reaction in detail ONe of HND

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Q: H2SO4 Он

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Q: Write the products of the following Cope rearrangements; pay particular attention to the…

A: Whenever there is the formation of a product in which the two same groups are in the same plane,…

Q: ? つ Ho

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Q: The first alkene which requires the position of the double bond to be indicated is?

A: Alkene contains a carbon-carbon double bond and for this minimum two carbon atoms are required.

Q: How to synthesize 1-phenyl-1-bromopropane from benzene?

A: The 1-phenyl-1-brmopropane is an important product obtained from benzene through a series of two…

Q: Cyclohexene reacts with bromine in the presence of NaI to yield -?

A: The reaction of cyclohexene with bromine in the presence of NaI proceeds through two steps. In the…

Q: Br NACN CH3CN

A: The reaction undergo bimolecular nucleophilic substitution reaction with inversion of configuration.

Q: Give clear handwritten mechanism of the reactions and form major products possible!

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Q: Sinthesis of 2,3-diphenylquinoxaline: which produce as a by product? HCl NH3 H2 H2O

A: The structure of 2,3-diphenylquinoxaline is as follows:

Q: give the major products and include stereochemistry when appropriate

A: The question is based on the concept of organic reactions.   We have to identify the product formed…

Q: How would I produce ethoxybenzene from benzene

A: Answer:- this question is answered by using the simple concept of preparation of ethoxybenzene from…

Q: give the major produc

A: 1. Baeyer -Villiger oxidation :  Ketone and per acid with acid reagent rearranges to esters is…

Q: Arrange the following in order of decreasing reactivity to nucleophilic addition: ketone, aldehyde.…

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Q: Starting with benzene and using any other necessary reagents of your choice, create a synthesis (or…

A: When benzene is treated with Chloro propane in presence of aluminium chloride, then Friedel crafts…

Q: Explains the general concept of the manufacture of benzene by dealkylation of toluene with hydrogen

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Q: Please show the reaction for the Alkene Halogenation and Explain each step in the reaction in great…

A: Alkenes react readily with chlorine or bromine, in dark, in a solvent such as CCl4 , to produce the…

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.