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Formation of esters (Esterification)
(1) The reaction is shifted to the right via using excess of alcohol or removal of water by distillation.
(2) The reactivity of alcohol towards esterification.
tert-alcohol < sec-alcohol < pri-alcohol < methyl alcohol
(3) The acidic strength of carboxylic acid plays just a minor role.R3CCOOH2CHCOOH2COOH3COOH
principle of qualitative analysis of funcional group
Compounds with similar molecular formula but different properties are known as Isomers and the phenomenon is known as Isomerism.
The lactone, a cyclic ester, can form an enolate ion, and this ion is alkylated by methyl iodide.
principle and application
It gives Meta Bromo Benzoic acid.
Reaction of ammonia with diborane at 475K gives a compound B3N3H6 known as borazine or borazole: Borazine is best prepared by reducing B-trichloroborazme with sodium borohy
How Ceriumis analyzed specrometrucally?
reactivity of f-block elements
show the mechanism
information of boron element
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