Explain Halogenation of Activated Benzenes ?

Q: what is the major product formed when toulene react with vinyl chloride?

A: Given: Toluene reacts with vinyl chloride.  To find: Major product formed from the above reaction.…

Q: How to convert isopropanol to 2-bromopropane via Apell reaction?

A:

Q: product

A: Dear student this question is related to organic chemistry.

Q: During sulphonation of benzene, H2SO4 generates the electrophile SO2 O "HSO4 O SO3 O +H O

A: In this question, we will Identify which electronphile is generated from sulphonation reaction on…

Q: What does alkyl halides gives on heating with dry Ag2O ?

A:

Q: Show how to convert ethylene to Bromoethane compound.

A: The reaction in which an electrophilic unsaturated bonds, say, double or triple bond, reacts with an…

Q: Table 7. Reaction with ammoniacal AgNO3 Description of ammoniacal AGNO3. SAMPLE OBSERVATIONS…

A: Acetylene reacts with ammoniacal Silver nitrate solution and forms acetylide Ppt.Acetylene hydrogen…

Q: The best reagent for preparing 1-propanol from propene is

A: The reaction explained in below

Q: explain why homolysis of the O-H bond in phenol requires considerably less energy than homolysis of…

A: a) O-H bond in phenol is more polar as compared to O-H bond in ethanol. This is because the…

Q: What hydrocarbon forms the following products after reaction first with ozone and then with dimethyl…

A: Hydrocarbon of (E) -3-allylidenecylopent-1-ene the given following products after reaction first…

Q: Explain Vinyl Halides and Aryl Halides ?

A: Aryl Halides - Compounds in which a halogen is bound to a sp2- hybridised carbon of an aromatic…

Q: products

A:

Q: What is the major organic product from the reaction of 1-pentyne with 1 mole of HBr?

A: Electrophilic addition of HX to Alkyne  Alkyne undergoes electrophilic addition in much the same…

Q: Explain Hydrogenation and Alkene Stability ?

A: Hydrogenation reactions are those reactions in which unsaturated hydrocarbons (alkenes) will undergo…

Q: Draw structural formulas for the product  of reaction of cyclopentadiene with   dienophile.

A: [4+2]-cycloaddition of a conjugated diene and a dienophile (an alkene or alkyne), an electrocyclic…

Q: Explain Secondary Alkyl Halides ?

A: Alkyl halides are the groups of hydrocarbons containing halogens.

Q: Explain the use of crown ethers in nucleophilic substitution reactions ?

A: Given Explain the use of crown ethers in nucleophilic substitution reactions ?

Q: Show how norbornane can be prepared from cyclopentadiene.

A: Norbornane can be prepared from cyclopentadiene through pericyclic reaction.

Q: Explain Allylic Carbocations in Biological Reactions ?

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Q: Explain the ortho-xylene oxidation reaction

A: The oxidation of o-xylene results in the formation of maleic anhydride, pthalide, o-tolualdehyde and…

Q: Discuss the electrophilic aromatic substitution of substituted benzenes ?

A: Electrophilic aromatic substitution is the type of reactions in which an electrophile is substituted…

Q: Using chemical equations, show how can you prepare:            3-pentene-1-ol using propyne and…

A: Terminal alkynes are considered to be sufficiently acidic to release H+ ions when treated with…

Q: Explain the mechanism for halogenation of alkenes ?

A: Halogenation of alkenes take place via addition reaction. Markonikov's addition reaction takes place…

Q: reaction the chloro-propyle with chloro-methyle by using Sodium metal as catalyst I .A ethane .B…

A: The given reaction is an example of Wurtz's reaction where two alkyl halides react to give a…

Q: Explain the characteristics of electrophilic addition of HX to alkenes ?

A: GIVEN: The determine the characteristics of electrophilic addition of HX to alkenes Explanation:…

Q: Draw structural formulas for the product  of reaction of cyclopentadiene with   dienophile.

A: The structural formula for the product of reaction of cyclopentadiene with the given dienophile has…

Q: catalytic hydrogenation.

A:

Q: what is the purpose of Dichlorocarbene Addition to an Alkene?

A: Dichlorocarbenes (CCl2) are reactive intermediates produced from chloroform (CHCl3). These are used…

Q: Account the solubility of carboxylic acids in distilled water

A: In this question, we will dicuss about the solubility of carboxylic acid in distilled water.  You…

Q: what is the difference between the cyclopentadienyl anion and pyrrole?

A: These two compounds are aromatic compounds. The cyclopentadiene is unusually acidic because loss of…

Q: Which product is formed by the bromination of 2-butene?

A: To solve this problem we will show the different products formed by the bromination of 2-butene .

Q: Explain  Chlorination Versus Bromination ?

A: In a reaction, if a bromine molecule is introduced then it is called a bromination whereas if…

Q: Effects of solvents on phenol halogenation

A: Halogenation of phenol depends on the solvent medium like water or less polar solvent we have taken.

Q: Draw structural formulas for the product  of reaction of cyclopentadiene with   dienophile.

A: The structural formulas for the product of the reaction of cyclopentadiene with a dienophile have to…

Q: what is the compound that most easily reacts with bromine in addition? a) CH4 b) C2H2 c) C3H8 d)…

A: The compounds are named as: a. CH4 - Methane b. C2H2 - Acetylene c. C3H8 - Propane d. C4H10 - Butane…

Q: What happens when benzene reacts with chlorine in the presence of sunlight?

A: Benzene will undergo addition reaction with Cl2 in presence of sunlight.

Q: What is the structural feature of hydrocarbons that can be oxidize by the Baeyer's reagent?

A: Baeyer's reagent is alkaline KMnO4 this reagent is used in laboratory to detect the presence of…

Q: Explain the Types of Pericyclic Reactions ?

A: A pericyclic reaction is an organic reaction where the transition state has cyclic geometry and the…

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.