What is the difference between an electrophilic addition and a nucleophilic addition? Is there a rule or easy to understand pattern that can be used to differentiate between the two types?
Electrophilic addition is where the group being added accepts an electron pair while nucleophilic addition is where the group being added donates an electron pair.
One way to do this is to look at the reaction mechanism and see if the electrons move from the group being added or to the group being added.
This is electrophilic addition because the
This is nucleophilic addition because the carbon atom in the
Another way to deduce if it's electrophilic or nucleophilic addition is to work out whether the atom that the group is being added to is electron deficient or not. This can be done by drawing dipoles onto molecules.
As you can see in the first mechanism, as the bromine molecule approaches the alkene, it has a dipole induced into it.
Thus, an electron pair from the
In the second mechanism, it's not the
One final thing to remember is that a nucleophile always has a lone pair of electrons will an electrophile doesn't.
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Electrophilic addition involves the addition of an electrophile to a molecule, typically an unsaturated organic compound. Nucleophilic addition, on the other hand, entails the addition of a nucleophile to a molecule. The key difference lies in the type of species added.
No specific rule or pattern universally differentiates the two types of additions, as they are defined by the nature of the reacting species. Understanding the roles of electrophiles (electron-seeking species) and nucleophiles (electron-donating species) in reactions is crucial for distinguishing between electrophilic and nucleophilic additions.
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When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
- Why do elimination reactions compete with substitution reactions when alkyl halides react with a nucleophile?
- Why do carbocations rearrange?
- What conditions are present to determine whether a reaction will be sn1 or sn2?
- If substitution of a nucleophile has happened, does that mean it is an E or an SN reaction?
- Regarding E2 reactions, predict the stereochemistry of the bromoalkene that would result from the loss of one mol of #HBr# from meso- and from (±)-1,2-dibromo-1,2-diphenylethane. Which reaction should be slower? Why?
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