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A step-by-step guide on how to determine degrees of unsaturation in organic chemistry, both from the molecular structure and the chemical formula. It explains that a degree of unsaturation corresponds to a deficiency of 2 hydrogen atoms, and provides rules for calculating unsaturations based on the presence of double bonds, rings, triple bonds, halogens, nitrogen, and oxygen in the molecular formula.
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# Unsaturations = Saturated # of H – Unsaturated # of H 2
Degrees of Unsaturation from Formula
Degrees of Unsaturation from Formula
Degrees of Unsaturation from Formula
Combined Example # Unsaturations = Saturated # of H – Unsaturated # of H 2
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