acid halides, Chemistry

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what are the properties of acid halides

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Characteristics of tautomerism - isomerism, Characteristics of tautomerism ...

Characteristics of tautomerism (a) Tautomerism (cationotropy) is caused by the oscillation of hydrogen atom between two polyvalent atoms present in the molecule. The modificati

Benzylic halide undergo sn1 or sn2 mechanism , Will benzylic halide undergo...

Will benzylic halide undergo SN1 or SN2 mechanism ?Why? Ans) Benzyl chloride is a  primary alkyl halide and undergo SN2 rapidly.

Entropy change for the reaction., The standard free energy change for a rea...

The standard free energy change for a reaction is -212.3 kJ mol -1 . If the enthalpy of the reaction is - 216.7 kJ mol -1 , calculate the entropy change for the reaction.

Show the basic stucture of esters, Q. Show the basic stucture of Esters? ...

Q. Show the basic stucture of Esters? Ans. Esters have the general formula RCOOR'. Both R and R' are alkyl groups. Esters have the ester functional group: Anima

What is alloys, Q. What is Alloys? Metals have a property of combining...

Q. What is Alloys? Metals have a property of combining with other metals to form alloys. An alloy may be defined as a solid which is formed by a combination of two or more met

Free radical addition reactions - organic chemistry, Free radical addition ...

Free radical addition reactions: Those reactions that include the initial attack by a free radical are termed as free radical reactions. Inculcation of hydrogen bromide to alk

How tetrahedral complex splitting takes place?, The tetrahedral arrangement...

The tetrahedral arrangement of four ligands surrounding the metal ion may be visualized. It is clear that in tetrahedral field, none of the orbitals point exactly towards the ligan

Why does methyl ethanoate not give iodoform test?, Why does methyl ethanoat...

Why does methyl ethanoate not give iodoform test while ethyl ethanoate does? Ans) Iodoform test for esters is the test given by its products on hydrolysis methyl ethanoate give

Organic chemistry, why isoquinoline is weak base as compare to quinoline?

why isoquinoline is weak base as compare to quinoline?

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