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How to find stability of carbocations in benzene ring..???How to find optically inactive isomers ??? (say of--C2H5Cl)How to find the weakest C-X (carbon-halogen bond in a benzene ring???? Solution) basically 3 degree carbocations are more stable as compared to 2 degree and one degree. for optically inactive isomer look for terms like racemic mixture and diastomers and the weakest halgon bond depends on leaving group halogen better leaving group weaker the bond
Saponification value - Analysis of oils and fats It is quantify of fatty acids denote as esters in oils and fats. It is described as the number of milligrams of KOH needed to s
reaction of mono hydric alcohol
Edible colours - Chemicals in food Edible colours employed for food are mainly dyes. The make use of food dyes is specifically wide spread. They are utilized to colour everythi
Q. What is Activation Energy? Ans. Colliding molecules which overcome the activation energy form an activated complex. In the activated complex, original bonds are partial
(a) Co-ordination compound A co-ordination compound contains a central metal atom or cation which is surrounded by a suitable number of anions or neutral molecules and usually re
Advantages of radiometric titration
Preparation of dihydric alcohols
Explain in words why hydroboration leads to anti-Markovnikov addition of hydrogen whereas most electrophilic addtions to alkenes result in Markovnikov addition.
How to prepare my seminar paper ?
Ethylbenzene Ethylbenzene has a three-proton triplet and, at somewhat greater chemical shift, in the benzylic proton region, a two-proton quartet. p-Xylene has a six-proton si
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