These MP Board Class 11th Chemistry Notes for Chapter 12 Organic Chemistry: Some Basic Principles and Techniques help students to get a brief overview of all the concepts.
MP Board Class 11th Chemistry Notes Chapter 12 Organic Chemistry: Some Basic Principles and Techniques
→ Isomerism : Two or more compounds which are different in their properties but have same molecular formula, are called isomers and this phenomenon is called isomerism.
→ Types:
- Chain isomerism : When difference exists in chain of carbon atoms.
- Position isomerism : When functional group is attached in different positions in same chain.
- Functional isomerism : When functional groups are different.
- Metamerism : Functional group is same but alkyl groups attached with it are different.
- Tautomerism : Special type of functional group isomerism in which both the isomers of a compound are in dynamic equilibrium.
- Ring chain isomerism : Structure of compound is open chain or cyclic.
- Optical: Formation of enantiomers of different optical properties by chiral molecules, (viii) Geometrical: Formation of cis-trans isomers due to restricted rotation in compounds of C = C double bond.
- Conformation : Formation of various spatial arrangements due to free rotation around C—C single bond.
→ Alkane : Saturated hydrocarbon, paraffin (less reactive) general formula C„H2)1+2, regular tetrahedral structure, H—C—H bond angle 109°28′ and sp3 hybridization in C-atom.
→ Conformation in ethane : Two forms (i) Eclipsed : In which H-atoms attached to both carbon are in front of each other.
(ii) Staggered : In which H-atoms of both carbon are in between each other. Low energy and more stable.
→ Conformation of cyclohexane: Two forms (i) Chair or staggered and (ii) Boat or eclipsed.
→ Chirality : Such compounds whose mirror images are non-superimposed.
→ Asymmetric carbon atom : Such a carbon atom to which four different groups are linked.
→ Optical isomers: Compounds which rotate the plane polarized to opposite direction and are mirror image of each other.
→ d – or (+) form : Which rotates the plane polarized light to the right.
Organic compounds of carbon : Compounds of carbon and hydrogen or their derivatives which have carbon-carbon bond.
→ Alkyl radicals : Part of molecule after ignoring one hydrogen atom in paraffin hydrocarbon.
→ Functional group : Atom or group of atoms determining the general chemical properties of the organic compound.
→ Homologous series : Series of compounds having common functional group and composed by the difference of —CH2
→ Nomenclature of organic compounds : IUPAC system.
→ l-(or) (-) form : Which rotates the plane polarised light to the left.
→ Racemic mixture : Equimolar proportion of d- and l-form is optically inactive.
→ Inductive effect is pennanent displacement of electrons along the chain of C-atoms.
→ Electromeric effect is temporary effect and occurs at the requirement of attacking species.
→ Resonance effect results in generation of centres of high and low electron density in a mol-ecule.
→ Free radical: Obtained by heterolytic cleavage. No charge but contain unpaired electron.
→ Carbocation : Positively charged carbon atom or group.
→ Carbanion : When negative charge is on carbon atom.
→ Meso form : Molecule with one or more chiral centre which is optically inactive due to internal arrangement.
→ Alkene : Carbon atoms of double bond is sp2 hybridized. One cr and 7t-bond is in between carbon. These can show chain, position and geometrical isomerism. General formula CnH2n
→ Alkyne : Carbon atoms of triple bonds are sp hybridized and are linear molecules with bond angle 180°. General formula CnH2n-2. These show chain and position isomerism.
→ Arene : Aromatic hydrocarbons which contain benzene ring. Each carbon atom in benzene is sp2 hybridized in which each bond angle is 120°.
→ Isomerism in Arenes : They have position isomerism. Disubstituted benzene occur in three isomeric forms (ortho, meta and para).
→ Crystallisation:
(a) Simple crystallisation : When hot saturated solution of any substance in a suitable sol-vent is cooled slowly, solid crystalline pure substance is obtained.
(b) Fractional crystallisation : Substances of different solubilities crystallise one by one from the solution which contains two or more than two substances as solute. Substance with least solubility crystallise first.
→ Sublimation : On heating, solid substance directly changes into gaseous state without chang-ing into liquid state and vice-versa.
→ Distillation : The process in which a liquid changes into vapour state and again it condenses back to liquid state. ’
→ Fractional distillation : Mixture of liquids which differ sufficiently in their melting points distil at different temperature. The liquid with low melting point distil first.
→ Steam distillation : Liquids having boiling point less than 100°C and immiscible with water, distil with steam. When condensed, different layers can be separated by separating funnel.