Carbon: The Basis of Molecular Diversity

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Last updated 10:14 PM on 7/6/26
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24 Terms

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Organic chemistry

The study of carbon-containing compounds

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Why is carbon central to biological diversity?

It has 4 valence electrons, so each carbon atom can form 4 covalent bonds, allowing huge variety in molecular shape & size

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Valence of carbon

4

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Shape of methane

Tetrahedral

<p>Tetrahedral</p>
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Shape around a carbon-carbon double bond

Flat/planar

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Hydrocarbons

Organic molecule made up of only carbon and hydrogen

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Are hydrocarbons polar or nonpolar?

Nonpolar and hydrophobic, because C-H bonds share electrons equally

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Isomers

Compounds with same molecular formula but different structural formula = different properties

<p>Compounds with same molecular formula but different structural formula = different properties</p>
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Structural isomers

Isomers that differ in covalent arrangement of their atoms e.g. Straight vs branched

<p>Isomers that differ in covalent arrangement of their atoms e.g. Straight vs branched</p>
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Cis-trans isomers

Isomers with same structural formula but different spatial arrangement around a double bond (rotation is restricted)

<p>Isomers with same structural formula but different spatial arrangement around a double bond (rotation is restricted)</p>
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Cis isomer

A double-bond isomer where the two reference groups are on the same side

<p>A double-bond isomer where the two reference groups are on the same side</p>
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Trans isomer

A double-bond isomer where the two reference groups are on opposite sides

<p>A double-bond isomer where the two reference groups are on opposite sides</p>
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Enantiomers

Isomers that are mirror images of each other, due to an asymmetric carbon

<p>Isomers that are mirror images of each other, due to an asymmetric carbon</p>
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Asymmetric carbon

A central carbon atom bonded to four different groups

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Functional group

A group of atoms attached to a carbon skeleton that takes part in chemical reactions and affects the molecule's properties

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  • Hydroxyl group (-OH)

  • Polar

  • Found in alcohols

  • Forms hydrogen bonds with water

  • Helps dissolve compounds

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Carbonyl group (C=O)

  • Found within a chain in ketones

  • Found at end of chain in aldehydes

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Carboxyl group (-COOH)

  • Acts as an acid — can donate an H⁺

  • Found in carboxylic (organic) acids.

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Amino group (-NH2)

  • Acts as a base — can accept an H⁺

  • Found in amines and amino acids

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Sulfhydryl group (-SH)

  • Found in thiols

  • Two -SH groups can form a cross-link that stabilises protein structure

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Phosphate group (–OPO3²⁻)

  • Adds negative charge to a molecule

  • Involved in energy-releasing reactions (e.g. in ATP)

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Methyl group (-CH3)

Nonreactive

Acts as a molecular tag that can affect gene expression and molecular shape

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ATP (adenosine triphosphate)

Adenosine attached to 3 phosphate groups - the main energy-carrying molecule in cells

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What happens when ATP reacts with water?

It loses one phosphate group, becoming ADP + inorganic phosphate (Pi), and releases energy