A general overview of what happens in an elimination reaction.
The mechanism and rate law for an E2 reaction are described.
This video looks at how the leaving group affects the regioselectivity of E2 reaction.
Here we look at how having Br, Cl or I as a leaving group affects the regioselectivity of an E2 reaction and the major product prediction.
Here we look at how having F as a leaving group affects the regioselectivity of an E2 reaction and the major product prediction.
Here we look at important factors to look at when deciding which product is the most stable alkene.
This video discusses how you would predict the major product, keeping regioselectivity and stereoselectivity in mind, when the beta carbon active in the reaction has only one hydrogen bonded to it.
This video discusses how you would predict the major product, keeping regioselectivity and stereoselectivity in mind, when the beta carbon active in the reaction has two hydrogens bonded to it.
In this video we look at the requirements for an E2 reaction to occur with a cyclohexane and we look at three example of product prediction.
In this video we look at how stereoselectivity comes into play when determining the major product of an E2 reaction.
This video discusses the conformational needs for an E2 reaction to occur.
We will be looking at factors (other than the concentration of the alkyl halide and the base) that affect how quickly the reaction proceeds for an E2 reaction.
The mechanism and rate law for an E1 reaction are described.
We will be looking at factors (other than the concentration of the alkyl halide) that affect how quickly the reaction proceeds for an E1 reaction.
We look at how regioselectivity and stereoselectivity affect the prediction of the major species in an E1 reaction.
We look at an example problem in this video applying the idea of regioselectivity ans stereoselectivity to identify the major product.
We look at how an E1 reaction proceeds for a cyclohexane.