What is the Difference Between Pyridine and Pyrimidine?
🆚 Go to Comparative Table 🆚Pyridine and pyrimidine are both heterocyclic organic compounds with cyclic structures containing carbon and nitrogen atoms. However, there are some key differences between them:
- Nitrogen Atoms: Pyridine consists of one nitrogen atom, while pyrimidine has two nitrogen atoms in its structure.
- Chemical Formula: Pyridine has the chemical formula C5H5N, and its structure resembles benzene with one methyl group replaced by a nitrogen atom. Pyrimidine has the chemical formula C4H4N2 and is one of the three diazines (six-membered heterocyclics with two nitrogen atoms in the ring).
- Basicity: Pyrimidine is less basic than pyridine due to the inductive, electron-withdrawing effect of the second nitrogen atom. The pKa value for protonated pyrimidine is 1.23, compared to 5.30 for pyridine.
- Electrophilic Substitution: Electrophilic substitution of pyrimidine is less facile than that of pyridine because of the decreased basicity compared to pyridine. However, the 5-position on the pyrimidine ring is less electron deficient, and substituents there are quite stable, leading to relatively facile electrophilic substitution at the 5-position, including nitration and halogenation.
- Occurrence in Nucleic Acids: In nucleic acids, three types of nucleobases are pyrimidine derivatives: cytosine (C), thymine (T), and uracil (U).
On this pageWhat is the Difference Between Pyridine and Pyrimidine? Comparative Table: Pyridine vs Pyrimidine
Comparative Table: Pyridine vs Pyrimidine
Pyridine and pyrimidine are both heterocyclic organic compounds with a benzene-like structure, but they have some differences in their structure and properties. Here is a comparison table highlighting the differences between pyridine and pyrimidine:
Feature | Pyridine | Pyrimidine |
---|---|---|
Chemical Formula | C5H5N | Not specified, but analogous to pyridine |
Structure | Resembles benzene with one methyl group replaced by a nitrogen atom | Resembles benzene with two methyl groups replaced by nitrogen atoms |
Number of Nitrogen Atoms | One | Two |
Basicity | Weaker base than pyrimidine | Less basic than pyridine |
Electrophilic Substitution | Easier than pyrimidine | Less facile than pyridine |
Pyridine is a weak alkaline and exists in the liquid state, while pyrimidine is less basic than pyridine due to the inductive, electron-withdrawing effect of the second nitrogen atom. Additionally, the decreased basicity of pyrimidine compared to pyridine makes electrophilic substitution of pyrimidine less facile.
Read more:
- Purine vs Pyrimidine
- Pyrrole Pyridine vs Piperidine
- Purine vs Pyrimidine Synthesis
- Pyrrolidine vs Piperidine
- Thymine vs Thymidine
- Pyridoxal vs Pyridoxamine
- Cytosine vs Thymine
- Pyrrole Furan vs Thiophene
- Thymine vs Uracil
- Furanose vs Pyranose
- Cytosine vs Cysteine
- Porphyrin vs Protoporphyrin
- Pyruvate vs Pyruvic Acid
- Adenosine vs Adenine
- Quinoline vs Isoquinoline
- DNA vs RNA Nucleotide
- Azomethines vs Ketimines
- Hexose vs Pentose
- Pyridoxal 5 Phosphate vs Pyridoxine Hydrochloride