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AnswerQuestion Answers for Class 12Class 12 BiologyClass 12 ChemistryClass 12 EnglishClass 12 MathsClass 12 PhysicsClass 12 Social ScienceClass 12 Business StudiesClass 12 EconomicsQuestion Answers for Class 11Class 11 EconomicsClass 11 Computer ScienceClass 11 BiologyClass 11 ChemistryClass 11 EnglishClass 11 MathsClass 11 PhysicsClass 11 Social ScienceClass 11 AccountancyClass 11 Business StudiesQuestion Answers for Class 10Class 10 ScienceClass 10 EnglishClass 10 MathsClass 10 Social ScienceClass 10 General KnowledgeQuestion Answers for Class 9Class 9 General KnowledgeClass 9 ScienceClass 9 EnglishClass 9 MathsClass 9 Social ScienceQuestion Answers for Class 8Class 8 ScienceClass 8 EnglishClass 8 MathsClass 8 Social ScienceQuestion Answers for Class 7Class 7 ScienceClass 7 EnglishClass 7 MathsClass 7 Social ScienceQuestion Answers for Class 6Class 6 ScienceClass 6 EnglishClass 6 MathsClass 6 Social ScienceQuestion Answers for Class 5Class 5 ScienceClass 5 EnglishClass 5 MathsClass 5 Social ScienceQuestion Answers for Class 4Class 4 ScienceClass 4 EnglishClass 4 MathsWhat do you mean by anomeric carbon? I want an answer preferably for anomeric carbon in carbohydrates (sugars). AnswerVerified511.8k+ viewsHint: Anomers are epimers of cyclic monosaccharides or glycosides that differ in their C-1 configuration if they are aldoses, or their C-2 configuration if they are ketoses. Anomeric carbon or anomeric core refers to the anomeric carbon in anomers.Complete answer:The carbon derived from the carbonyl carbon (the ketone or aldehyde functional group) of the open-chain form of the carbohydrate molecule is known as the anomeric carbon. The method of converting one anomer to the other is known as anomerization.The anomeric carbon in the cyclic form of sugar is the carbon that was previously part of the carbonyl group in the straight-chain structure.C1 becomes a chiral centre when the chain becomes a coil.The anomeric carbon is C1.The carbonyl group in D-fructose is at C2.C2 is the anomeric carbon in this case.Or The carbon in a monosaccharide (such as glucose) that rotates is an example of anomeric carbon. The carbon (C) connected to two oxygen (O) atoms joined by single bonds determines the anomeric carbon. This rotation results in the formation of two distinct configurations: and -anomers. Carbohydrates can then switch between the and configurations on their own: mutarotation is a term used to describe a mechanism.Note: The electronic effect, which is an interaction of the orbitals of the ring O and the substituent bond, causes anomeric carbon to be reactive. The anomeric centre is critical for carbohydrate reactivity because it is where the ring opens, forming the carbonyl group, which is an important functional group.Recently Updated PagesMaster Class 11 English: Engaging Questions & Answers for SuccessMaster Class 11 Biology: Engaging Questions & Answers for SuccessMaster Class 11 Physics: Engaging Questions & Answers for SuccessMaster Class 11 Maths: Engaging Questions & Answers for SuccessMaster Class 11 Accountancy: Engaging Questions & Answers for SuccessClass 11 Question and Answer - Your Ultimate Solutions GuideMaster Class 11 English: Engaging Questions & Answers for SuccessMaster Class 11 Biology: Engaging Questions & Answers for SuccessMaster Class 11 Physics: Engaging Questions & Answers for SuccessMaster Class 11 Maths: Engaging Questions & Answers for SuccessMaster Class 11 Accountancy: Engaging Questions & Answers for SuccessClass 11 Question and Answer - Your Ultimate Solutions Guide

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