A structural formula represents how chemical atoms in a molecule are connected. It adds information that a molecular formula alone does not provide. Depending on the notation, bonds and grouped atoms may be drawn explicitly or represented in a condensed structural formula.[ref]
IUPAC Compendium of Chemical Terminology, fifth edition (Gold Book) by International Union of Pure and Applied Chemistry. Entry S06061, structural formula: information about atom connectivity; DOI10.1351/goldbook.S06061.
For ethanol, can be unpacked as a carbon with three hydrogens, joined to a carbon with two hydrogens, joined to oxygen, joined to hydrogen. Counting the groups recovers , since . That count is a useful check, but it discards the connectivity information that distinguishes ethanol from dimethyl ether, .
A structural drawing also needs a clear convention about spatial meaning. A plain line usually represents a chemical bond, rather than a measured length on the page. Rotating the paper does not change the represented molecule. If a drawing is intended to specify a three-dimensional configuration, the additional conventions belong to stereochemistry; a connectivity formula should not silently be treated as complete molecular geometry.
A condensed structural formula writes connected groups of chemical atoms compactly, omitting some explicit bond strokes. It preserves interpretable connectivity information, unlike a molecular formula that merely totals the atoms. It is one way to represent a structural formula, whose purpose is to describe how atoms are connected.[ref]
IUPAC Compendium of Chemical Terminology, fifth edition (Gold Book) by International Union of Pure and Applied Chemistry. Entry S06061, structural formula: connectivity information; DOI10.1351/goldbook.S06061.
For an original counting example,can be unrolled as . The two terminal groups supply two carbons and six hydrogens; four interior groups supply four carbons and eight hydrogens. Thus the molecular formula is , since and . The parentheses abbreviate a connected repeated group, rather than introducing a separately floating molecule.
The compression must be interpreted with the chosen convention. A formula such as specifies different connectivity from despite their common atom counts. Neither expression by itself gives every bond angle or a unique three-dimensional conformation; those questions involve molecular geometry and stereochemistry.
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