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Fischer Esterification
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The organic reaction in which a carboxylic
acids reacts with excess alcohol in presence of a strong acid catalyst
to form an ester.This reaction is known as Fischer Esterification.
Carbohydrates Assignment -02 1. Explain the Ring Structure and Determination of Ring size of Glucose 2. Explain the following conversions A) D-Glucose to D-Fructose B) D-Fructose to D-Glucose 3. What is Anomer and Epimer ? MID EXAMINATION-02 (20 Marks) 1. Explain the structure of Glucose (10 M) 2.Explain the Structure of Fructose(5 M) 3. what is a Killiani-Fischers synthesis(5 M) Dr Sateesh Kumar Beepala Assistant Professor in Chemistry GDC Tekkali
methylcyclohexane conformations: 1) Methylcyclohexane is cyclohexane in which one hydrogen atom is replaced with a methyl group substituent. 2) Methylcyclohexane can adopt two basic chair conformations: one in which the methyl group is axial, and one in which it is equatorial . 3) The most stable conformation of methylcyclohexane is the chair conformation in which the methyl group is equatorial. 4) The alternative chair conformation, in which the methyl group is axial, is 7.3 kJ/mol higher in energy. 5) This difference corresponds to a equatorial:axial conformer ratio of 19:1 at 25 °C.
Organo Metallic Compounds Assignment -03 1) what is Organo metallic compound and explain its Classification 2) What is 18 e- rule and explain with an example 3) Define hapticity? by ...
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