Why carboxylate salts less reactive than esters, Chemistry

Assignment Help:

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;

 


Related Discussions:- Why carboxylate salts less reactive than esters

Step growth or condensation polymerisation, Step growth or condensation pol...

Step growth or condensation polymerisation In this form of polymerisation monomers usually consist of two functional sets, that is difunctional monomers. In that method no init

Calomel electrode, Construction and working of calomel electrode with a lab...

Construction and working of calomel electrode with a labelled diagram

Homework, silicon carbide is prepared using the chemical reaction SiO2+3C p...

silicon carbide is prepared using the chemical reaction SiO2+3C producing SiC+2CO so how many grams of SiC can be produced from 15 grams of C

Solubility Product Constant , The known metal ion solution used contains 0....

The known metal ion solution used contains 0.10 M of each of the six metal ions (i.e. 0.10 M Ag+ and 0.10M Pb2+). An equal volume of 3 M HCl and the known solution are mixed. What

Determine atomic number and electrons of an element, The atomic number of a...

The atomic number of an element is 35. What is the total number of electrons present in all the p-orbitals of the ground state atom of that element: (1) 6        (2) 11

Phenol, what is the acidity of phenol?

what is the acidity of phenol?

Write Your Message!

Captcha
Free Assignment Quote

Assured A++ Grade

Get guaranteed satisfaction & time on delivery in every assignment order you paid with us! We ensure premium quality solution document along with free turntin report!

All rights reserved! Copyrights ©2019-2020 ExpertsMind IT Educational Pvt Ltd