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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
write about deutorium
Uses of Oxalic acid or Polyprotic acid (i) Oxalic acid is used in the manufacture of carbon monoxide, formic acid and allyl alcohol. (b) Oxalic acid is used as a laboratory
Q. Describe Coordinated octahedral complexes? Six-coordinated octahedral complexes of the type Mubr, Ma 3 b 3 , Ma 3 b 2 c, Ma 3 bcd, Ma 2 bcd, Ma 2 bcde, Mabcd of would all g
Time taken for an electron to complete one revolution in the Bohr orbit of hydrogen atom is: (1) 4 Π mr 2 / nh (2) nh/ 4Π 2 mr (3) nh/ 4Π 2 mr 2
1. Wet air containing 4.0 mole% water vapor at 76°F and 14.8 psia is passed through a column of calcium chloride pellets. The pellets absorb 97% of the water and none of the oth
Applications of hybridisation - Size of the hybrid orbitals As s- orbitals are closer to the nucleus than p- orbitals, it is reasonable to suppose that greater the s character
lithium and beryllium markedly differ from others members of their respective group
Explain The compound decarboxylates The compound decarboxylates; it is a disubstituted malonic acid in which the two a substituents are connected within a ring. The net effect
CAN SOMEONE PLEASE EXPLAIN TO BE HOW THE LIBERMANNS CHEMICAL REACTION WORKS? I ALSO NEED ALOT ABOUT THE CHEMISTRY BEHIND THE REACTION, AND CANT FIND MUCH ONLINE.. PLEASE HELP ME
classification
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