Reaction types

2. / Negatively charged carbon is in sp3 state.
6. effect / It is a temporary effect produced in presence of reagent only.
9. / This free radical is most stable.
10. effect / This effect is of great importance in conjugated compounds.
12. effect / This effect involves displacement of sigma electrons.
14. rearrangement / It is the reaction of an enolizable ester with a strong base to give a β-ketoester.
15. / another name for no-bond resonance effect.
17. fission / In this fission the bond breaks in such a way that each of the bonded atoms gets one electron of the shared pair.
18. reaction / It is a type of organic reaction in which two substituents are removed from a molecule in either a one- or two-step mechanism.
19. group / Example of group exhibiting plus R effect.
20. carbon / This carbon has maximum plus inductive effect.

1. reaction / a chemical reaction during which one functional group in a chemical compound is replaced by another functional group.
3. radical / Electrically neutral group having unpaired electrons
4. / Hyperconjugation explain the stability of these hydrocarbons.
5. fission / In this bond breaks in such a way that both the electrons remain with one of the atoms.
7. / Species having a carbon atom bearing positive charge.
8. / These are electron loving species.
11. reaction / reaction common in compounds that have unsaturated C-C bond, like double (alkene) and triple (alkyne) bonds.
13. / Number of hyperconjugating structure in ethyl carbonium ion
16. / covalent compounds that exhibit inductive effect.