Organic Chemistry

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20 Terms

1

Structural Diagrams

Different representations of organic molecules that convey chemical and physical properties.

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2

Hybridisation

The process by which atomic orbitals combine to form new hybrid orbitals in organic molecules.

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3

Acidity

The ability of a molecule to donate a proton (H+); more stable anions increase acidity.

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4

Lewis Acid

A molecular entity that acts as an electron-pair acceptor.

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5

Resonance

The delocalisation of electrons within a π-system, leading to increased stability of molecular structures.

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6

pKa

The negative logarithm of the acid dissociation constant (Ka); a more convenient measure of acidity.

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7

Hückel's Rule

A rule stating that cyclic, conjugated molecules exhibit aromaticity if they have (4n + 2) π-electrons.

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8

Chirality

A property of molecules that have non-superimposable mirror images, leading to enantiomers.

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9

Enantiomers

Non-superimposable mirror images of chiral molecules.

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10

Diastereoisomers

Stereoisomers that are not mirror images of each other.

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11

Stereogenic Centre

An atom with four different substituents, responsible for the chirality of a molecule.

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12

Conformational Isomers

Different spatial arrangements of molecules that result from rotation about single bonds.

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13

Optical Activity

The ability of chiral substances to rotate the plane of polarized light.

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14

Acidity and Basicity in Organic Chemistry

Key concepts involving the donation and acceptance of protons by molecular species.

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15

Cyclic Conjugated Structure

A structure where alternating double bonds allow for delocalisation of electrons, crucial for aromaticity.

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16

Amide Bond

A bond formed between an amine and a carboxylic acid; characterized by resonance stabilization.

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17

Peptide Bond

A specific type of amide bond linking amino acids in proteins.

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18

Stereoisomers

Compounds with the same molecular formula and connectivity but different spatial arrangements.

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19

1:1 Racemic Mixture

A sample containing equal amounts of both enantiomers of a chiral molecule.

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20

Geometric Isomers

Isomers that differ in arrangement across a double bond, categorized as cis or trans.

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