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carbohydrates: monosaccharides. oligo
carbohydrates: monosaccharides. oligo

lecture 2 - alcohols-ethers
lecture 2 - alcohols-ethers

CHM 103 Lecture 24 S07
CHM 103 Lecture 24 S07

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... Now, cancel the species that appear on both sides of the equation: Finally, since we know that the reaction takes place in basic solution, we must add 2 OH – ions to both sides of the equation to neutralize the 2 H+ ions on the right giving 2 additional H2O. The final net ionic equation, balanced fo ...
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... 25. (i) Low bond dissociation enthalpy and high hydration (solvation) enthalpy. or highest S.R.P. value among the halogens. (1) (ii) Due to its high electronegativity. (1) (3) (iii) Higher the oxidation state of chlorine in oxo acid, stronger the acid. (1) 26. (a) (i) To remove HX formed so that the ...
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... Grignard Reactions with Acid Chlorides and Esters • Use two moles of Grignard reagent. • The product is a tertiary alcohol with two identical alkyl groups. • Reaction with one mole of Grignard reagent produces a ketone intermediate, which reacts with the second mole of Grignard reagent. Chapter 10 ...
Kinetic studies on the oxidation of cyclohexanone by potassium
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... Pyrole  and  Imidazole   •  Pyrole  is  an  amine  and  a  conjugated  diene,          however  its  chemical  proper7es  are  not   consistent  with  either  of  these  structural  features   ...
Organic Chemistry, 11th Edition
Organic Chemistry, 11th Edition

... COVER IMAGE © Gerhard Schulz/Age Fotostock America, Inc.  ...
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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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