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0 votes
1 answer
120 views

Why does alpha-carbon substituents increase the rate of E2 reactions?

The reason for more reactivity of more substituted alkyl halides for E2 Reaction is said to be due to the more stability of its more substituted alkene character having transition state but here (...
D13G's user avatar
  • 89
3 votes
2 answers
223 views

NMR and dienes to isolate certain isotopes?

I am looking to achieve isotope separation using transition states. In the rxn of dienes with halogens, based on the temperature, the dienes can create a thermodynamic product or a kinetic product. ...
Young Jun Lee's user avatar
1 vote
0 answers
52 views

Investigating the effect of solvents (protic vs aprotic) on the alkaline hydrolysis of ethyl acetate using a conductivity meter

What different areas about solvents can be explored with the conductivities collected of the alkaline hydrolysis of ethyl acetate in propanone and ethanol? $$\ce{CH3COOC2H5 + NaOH -> CH3COONa + ...
Faisal Zia's user avatar
2 votes
1 answer
2k views

Kinetic vs thermodynamic control of HBr to 1,3-Butadiene

The author claims that the transition state leading to the formation of the 1,2 product from the allylic carbocation is lower in energy since the carbon (which is attached to Br in the 1,2 product) is ...
xasthor's user avatar
  • 1,632
26 votes
2 answers
1k views

Ambimodal transition states in some organic reaction pathways

In many computational studies, mechanisms appear to have so-called ambimodal transition states, i.e. a transition state which can lead to multiple products, in conflict to the common undergraduate ...
NotEvans.'s user avatar
  • 17.2k