Pharmaceutical Organic Chemistry I Lecture 2 (12 OCT) PDF

Summary

This lecture covers the basic concepts of alkanes, cycloalkanes, and their chemical properties including nomenclature. The document includes different types of chemical reactions, relevant diagrams and examples.

Full Transcript

Pharmaceutical Organic Chemistry I (PMC 102) Dr. Asmaa Yassen gu.edu.eg Quiz 02 Alkanes What is Alkane? Saturated Hydrocarbons General formula: CnH2n+2. contain only single bonds Names of Small Hydrocarbons No. of Carbons Formula Name (CnH2n+...

Pharmaceutical Organic Chemistry I (PMC 102) Dr. Asmaa Yassen gu.edu.eg Quiz 02 Alkanes What is Alkane? Saturated Hydrocarbons General formula: CnH2n+2. contain only single bonds Names of Small Hydrocarbons No. of Carbons Formula Name (CnH2n+2) 1 Methane CH4 2 Ethane C2H6 3 Propane C3H8 4 Butane C4H10 5 Pentane C5H12 6 Hexane C6H14 7 Heptane C7H16 8 Octane C8H18 9 Nonane C9H20 10 Decane C10H22 Methane, Ethane, Propane & Butane Alkane Alkyl group CH4 CH3 - Methane Methyl CH3CH3 CH3CH2 Ethane Ethyl H3C CH3 H3C C H2 H3C CH3 Propane propyl isopropyl CH3 CH2 CH3 H3C H3C H3C butane butyl sec-butyl CH3 CH3 CH3 H3C CH3 H3C CH3 H3C CH2 isobutane isobutyl tert-butyl Nomenclature of substituted alkanes Names of Common Substituent Groups What is the name for the following compound? Physical Properties of Alkanes 1. C1-C5 are gases at room temperature. 2. C6-C10 are Liquids. 3. Higher that C11 are semisolids or waxy matters. 4. Because they are non-polar, alkanes are insoluble in water but soluble in no- polar solvents. 5. Boiling points of liquid alkanes increase with increase molecular weight (increase with increasing number of carbons (more atoms, more electrons, more opportunities for induced dipole-induced dipole forces ). 6. Boiling points decreases with chain branching. As branching increases, the distances between the molecules increased and hence the Van-der Waal forces decreased leading to lowering the boiling point of the branched alkanes. Preparation Cycloalkanes are a class of hydrocarbons with carbon atoms connected in a ring structure. Formula: CnH2n The physical properties of cycloalkanes exhibit similarity to those of alkanes with open chains. Cycloalkanes exhibit a higher level of reactivity in comparison to alkanes because of angle strain in ring. Angle Strain Angle strain is the increase in potential energy of a molecule due to bond angles deviating from the ideal values. The ideal angle for cycloalkanes is 109.5°. cyclopropane is more highly strained, more unstable and more reactive and undergoes reaction. Cyclopentane (Bond angle = 108° ) and cyclohexane (Bond angle = 109.5 ° ) are not strained, stable. So, they are not reactive. The reactions of the cycloalkanes are generally just the same as the alkanes, with the exception of the very small ones - particularly cyclopropane. In the presence of UV light, cyclopropane will undergo substitution reactions with chlorine or bromine just like a non-cyclic alkane. Thank You

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