Knowee
Questions
Features
Study Tools

What is keto-enol tautomerism of nucleic acids?

Question

What is keto-enol tautomerism of nucleic acids?

🧐 Not the exact question you are looking for?Go ask a question

Solution

Keto-enol tautomerism is a phenomenon that occurs in nucleic acids. Nucleic acids are the building blocks of DNA and RNA, which are essential for storing and transmitting genetic information in living organisms.

Tautomerism refers to the interconversion of isomers, molecules that have the same chemical formula but different arrangements of atoms. In the case of keto-enol tautomerism, the isomers involved are the keto form and the enol form.

The keto form is the more stable and commonly observed form of nucleic acids. It has a carbonyl group (C=O) and a hydroxyl group (OH) attached to the same carbon atom. However, under certain conditions, such as changes in pH or temperature, the keto form can convert into the enol form.

The enol form is the less stable and less commonly observed form of nucleic acids. It has a double bond (C=C) and a hydroxyl group (OH) attached to the same carbon atom. The conversion from the keto form to the enol form involves the migration of a hydrogen atom and the rearrangement of bonds.

Keto-enol tautomerism is important in nucleic acids because it can affect their structure and function. The interconversion between the keto and enol forms can lead to changes in base pairing, which is crucial for the accurate replication and transcription of genetic information.

In summary, keto-enol tautomerism is a phenomenon in nucleic acids where the keto form and the enol form can interconvert. This tautomerism can have implications for the structure and function of nucleic acids.

This problem has been solved

Similar Questions

3. Discuss the keto-enol tautomerism in the hydrolysis of phosphoenolpyruvate

QuestionNo.13(Single Correct) A+ A-Marks : 4.00/ 1.00Which of the following keto gives most stable enol during tautomerism ?

What is tautomerisation?Select your answer:Select your answerOPTION ALTERNATIVE A 50:50 mix of enantiomers  The formation of a ketone  The formation of hemi-compounds The interconversion of two isomers  None of the above

Which of the following statements does NOT correctly describe a keto-enol tautomerism?A.The reaction results in a pi bond migration, forming a C=C double bond.B.The reaction can be acid-catalyzed by protonating an enol oxygen atom.C.The reaction involves removal of a proton from an α-carbon.D.The reaction results in an equilibrium mixture of keto and enol tautomers, which are constitutional isomers.

What name is given to nucleoside of DNA containing 2-deoxyribose and cytosine?

1/3

Upgrade your grade with Knowee

Get personalized homework help. Review tough concepts in more detail, or go deeper into your topic by exploring other relevant questions.