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Carboxylate salts
Carboxylate salts are less reactive than esters in nucleophilic acyl substitution reactions for two reasons. First, resonance stabilization of carboxylate salts is particularly significant because carboxylates have two identical, significant resonance structures;
Q. Illustrate Born-Haber cycle? Boron is always covalent and does not form,B 3+ ions, because' the energy required to remove three electrons is very high. Many simple compo
Visualisation of hybrid orbitals
assignments of hydrogen bonding
IUPAC System of Naming Organic Compounds In the IUPAC (International Union of Pure and Applied Chemistry) system, the name of an organic compound contain three parts that are:
HOW WE NAMING THE BOND LINE NOTATION
n-propyl acetate (bp 102 C) evaporates rapidly when exposed to air, but water(bp 100C)does not. Explain why
Illustrate resonance structures that define the electronic structure of benzene. Illustrate the structures of all conceivable disubstituted benzene isomers bearing two
Element is strongly electropositive and Y is strongly electronegative. Both element are univalent, the compounds formed from their combination will be: (1) X + Y -
1 gram of pure sodium carbonate is dissolved in water and the solution is made up to 50 ml of this solution 50 ml of 0.1 N HCl is added whose volume is 50 ml and the mixture furthe
Ask qwhy is 5-bromovanillin the major productuestion #Minimum 100 words accepted#
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