This mechanism is seen in Nucleophillic Substitution reactions, especially in those compounds in which the Carbon atom is more substituted . The rate of this mechanism depends on the step 1 where the leaving group leave with electron pair and leaves behind a carbocation. The whole rate depends only on one molecule. That’s why it
This is a type of reaction mechanism that is seen in case of nucleophillic substitution reactions. It is BIMOLECULAR NUCLEOPHILLIC SUBSTITUTION mechanism. In this kind of mechanism two molecules decide the rate of reaction, so it is BIMOLECULAR mechanism. The whole mechanism proceeds through a single step. That concerted step involves the bond breaking and
It is a type of condensation reaction that involves the condensation of an aldehyde or ketone with succinic ester in the presence of sodium ethoxide or Potassium ethoxide to yield unsaturated ester acid . The complete reaction is as below. The mechanism involves 3 steps , and firstly the succinate is treated with base to
Ald + ol Ald- Aldehyde ; ol – Alcohol. As the name suggests , this is a type of reaction which involve the formation of such a molecule which have “alcohol and aldehyde” functional groups.
How are reactions related to chemical bonds? The type of bond has a great effect on the rate of reaction or speed of reaction. Here we are going to discuss why and how it happens, First of all in case of ionic compounds:- Lets take example of Sodium hydroxide and Hydrochloric acid NaOH (aq) +