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A substitution reaction is also called a single displacement reaction, single replacement reaction, or single substitution reaction. Examples: CH3Cl reacted with a hydroxy ion (OH-) will produce CH3OH and chlorine. This substitution reaction replaces the chlorine atom on the original molecule with the hydroxy ion.
The obvious difference between substitution and elimination reactions is that substitution reactions replace one substituent with another while elimination reactions simply remove the substituent.
Often, in an sn1 reaction, the nucleophile is the solvent that the reaction is occurring in. Sn2: In sn2 reactions, the nucleophile displaces the leaving group, meaning it must be strong enough to do so. Often, this means that the nucleophile is charged \u2013 if not, then it must be a strong neutral nucleophile.
Look at the substrate. In the presence of a strong base, E2 will be the favored pathway. Elimination is typically preferred over substitution unless the reactant is a strong nucleophile, but weak base. Substitution is typically preferred over elimination unless a strong bulky base is used.
The main difference between substitution and elimination reactions is that substitution reaction proceeds with replacement with one another while elimination reactions proceed with the removal of atom or group.
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substitution reaction, any of a class of chemical reactions in which an atom, ion, or group of atoms or ions in a molecule is replaced by another atom, ion, or group.
An elimination reaction occurs when a reactant is broken up into two products. Elimination reactions occur with saturated compounds. The general equation for an elimination reaction: A \u2192 B+C. A substitution reaction occurs when an exchange of elements in the reactants takes place.
The main difference between addition and substitution reactions is that addition reactions involve the combination of two or more atoms or functional groups whereas substitution reactions involve the displacement of an atom or a functional group by another functional group.
1) E2 is a concerted mechanism where all the bonds are broken and formed in a single step. The E1, on the other hand, is a stepwise mechanism. 2) E2 reactions are favored by strong bases such as the methoxide (MeO\u2013), ethoxide (EtO\u2013), potassium tert-butoxide (tBuOK), DBN, DBU, LDA and etc.
An elimination reaction occurs when a reactant is broken up into two products. Elimination reactions occur with saturated compounds. The general equation for an elimination reaction: A \u2192 B+C. A substitution reaction occurs when an exchange of elements in the reactants takes place.

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