What is the Difference Between Chemoselectivity and Regioselectivity?
🆚 Go to Comparative Table 🆚Chemoselectivity and regioselectivity are two different chemical concepts in organic chemistry. The key difference between them is:
- Chemoselectivity refers to the preferential outcome of a chemical reaction among a set of possible alternative reactions. It involves the reactants preferring to react with one functional group over another in a substrate, even if more than one functional group is available to react.
- Regioselectivity refers to the preference of a chemical bond formation or a chemical bond cleavage in a reaction. This concept is used when a reaction has two or more possible products, and the possible products are regioisomers (also called constitutional isomers).
In summary:
- Chemoselectivity is about the reactants preferring one functional group over another in a substrate.
- Regioselectivity is about the preference of a chemical bond formation or a chemical bond cleavage in a reaction with two or more possible products that are regioisomers.
On this pageWhat is the Difference Between Chemoselectivity and Regioselectivity? Comparative Table: Chemoselectivity vs Regioselectivity
Comparative Table: Chemoselectivity vs Regioselectivity
Here is a table comparing chemoselectivity and regioselectivity:
Property | Chemoselectivity | Regioselectivity |
---|---|---|
Definition | Chemoselectivity refers to the preference of reactants for reacting with one functional group over another in a molecule. | Regioselectivity refers to the preference of a chemical bond formation or a chemical bond cleavage within a single functional group. |
Focus | The focus is on the specific functional group that the reactants prefer to react with. | The focus is on the specific location within a single functional group where a reaction occurs. |
Relation to Other Selectivities | Chemoselectivity can be related to stereoselectivity, which refers to the products of a reaction being stereoisomers. | Regioselectivity can be related to stereoselectivity, which refers to the preference of a chemical bond formation in a specific location within a single functional group. |
Examples | A reagent reacting preferentially with one functional group in a molecule containing multiple functional groups. | A reaction occurring at a specific site within a single functional group, such as the Markovnikoff addition. |
In summary, chemoselectivity is about the preference of reactants for specific functional groups, while regioselectivity is about the preference of a chemical bond formation or cleavage at a specific location within a single functional group.
Read more:
- Regioselectivity vs Stereoselectivity
- Stereospecific vs Stereoselective Reactions
- Specificity vs Selectivity
- Prochirality vs Prostereoisomerism
- Diastereomers vs Enantiomers
- Chemistry vs Biochemistry
- Electrophilic vs Nucleophilic Substitution
- Catalytic vs Stoichiometric Reagents
- Electrochemical Series vs Reactivity Series
- Chemistry vs Chemical Engineering
- Organic Chemistry vs Inorganic Chemistry
- Electrophoresis vs Chromatography
- Nucleophilicity vs Basicity
- Isomers vs Resonance
- Medicinal Chemistry vs Pharmaceutical Chemistry
- Synthesis Reaction vs Substitution Reaction
- Resonance vs Tautomerism
- Chemoorganotrophs vs Chemolithotrophs
- Photocatalysis vs Electrocatalysis