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Fundamentals of Organic Chemistry
Fundamentals of Organic Chemistry

... derivatives. The relationship of these compounds to biochemical is also discussed. Students registering for this course must also register for CHEM 2310L which is the laboratory component of the course. ...
Alcohols and Phenols
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Synthesis of Ketones and Aldehydes
Synthesis of Ketones and Aldehydes

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Carboxylic Derivatives - University of Nebraska Omaha
Carboxylic Derivatives - University of Nebraska Omaha

... • Nitriles are carboxylic acid derivatives; therefore, their names are based on the name of the corresponding carboxylic acid. • Nitriles are named by replacing the suffix “oic acid” with “enitrile”. • The prefix for functional group is cyano-. ...
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Aldehydes and Ketones

... Copyright © by Brooks/Cole Cengage Learning. All rights reserved. ...
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21:3 Classifying Chemical Reactions

Chapter 19. Aldehydes and Ketones: Nucleophilic Addition Reactions
Chapter 19. Aldehydes and Ketones: Nucleophilic Addition Reactions

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...  Addition yields a hydroxy ether, called a hemiacetal (reversible); further reaction can occur  Protonation of the OH and loss of water leads to an oxonium ion, R2C=OR+ to which a second alcohol adds to form the acetal ...
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main types and mechanisms of the reactions in organic chemistry
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Final Exam Review Sheet Chemistry 110a/1998
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... produced based on the limiting reactant.  If everything in the reaction went according to plan, and all of the reactant(s) reacted, this is how much product should be made.  This is NOT the same as the actual yield- amount that is produced based on an experiment  Error occurs, so actual yield is ...
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Asymmetric induction



Asymmetric induction (also enantioinduction) in stereochemistry describes the preferential formation in a chemical reaction of one enantiomer or diastereoisomer over the other as a result of the influence of a chiral feature present in the substrate, reagent, catalyst or environment. Asymmetric induction is a key element in asymmetric synthesis.Asymmetric induction was introduced by Hermann Emil Fischer based on his work on carbohydrates. Several types of induction exist.Internal asymmetric induction makes use of a chiral center bound to the reactive center through a covalent bond and remains so during the reaction. The starting material is often derived from chiral pool synthesis. In relayed asymmetric induction the chiral information is introduced in a separate step and removed again in a separate chemical reaction. Special synthons are called chiral auxiliaries. In external asymmetric induction chiral information is introduced in the transition state through a catalyst of chiral ligand. This method of asymmetric synthesis is economically most desirable.
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