Question
For each molecular formula below, calculate its degree of unsaturation and draw as many compatible structures as you can:
(a)
(b)
(c)
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Evidence boundary
This preserves all three formula calculations and the structure-drawing requirement of OpenStax Organic Chemistry Problem 7-1. The diagrams and enumeration are independently constructed and checked by carbon valence, implicit hydrogen counts, and graph cycles. They use conventional connected, neutral, closed-shell hydrocarbons; radicals, ions, disconnected fragments, and exotic bonding are outside this introductory scope. No spectra are supplied, so the structures are candidates rather than a uniquely identified compound.