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Chemistry

Chapter 15. Hydrocarbons

21 topics with concise breakdowns: definitions, key facts, and class questions.

This chapter is dedicated to the foundation of bioorganic chemistry — hydrocarbons. We will analyze compounds consisting only of carbon and hydrogen: alkanes, cycloalkanes, alkenes, alkadienes, alkynes, and arenes. They form the basic carbon skeleton of any biologically active molecule, from fatty acids to complex steroid hormones.

The section covers all key classes of hydrocarbons. You will study methods for their preparation (including the synthesis of higher cycloalkanes) and chemical properties. Special attention in the course is given to the concept of aromaticity in arenes, which is critical for understanding the structure of many drugs and DNA nitrogenous bases.

During seminars and colloquia, instructors most frequently ask about qualitative reactions (especially for alkynes and multiple bonds), mechanisms of addition and substitution reactions, and criteria for aromaticity. Confident mastery of these topics is your gateway to successfully learning biochemistry and pharmacology in senior years.

Section Topics

HydrocarbonsHydrocarbons are a crucial class of chemical substances determining the chAlkanesAlkanes are saturated hydrocarbons in which carbon atoms are bonded byPreparation of alkanesThe preparation of alkanes is traditionally divided into two broad cateChemical properties of alkanesSaturated hydrocarbons (alkanes) are characterized by extremely low reacCycloalkanesCycloalkanes are cyclic hydrocarbons with the general formula C_n H_{2nAlkenesAlkenes are unsaturated hydrocarbons whose molecules contain exactly onPreparation of alkenesAlkenes are prepared by eliminating atoms or entire groups from saturateChemical properties of alkenesAlkenes exhibit high chemical reactivity due to the presence of a doubleAlkadienesAlkadienes (diene hydrocarbons) are a class of hydrocarbons whose molecPreparation and properties of dienesDienes are organic compounds containing two double bonds. The most famoRubbersRubbers are elastic polymers whose molecules can stretch and return to AlkynesAlkynes are a homologous series of unsaturated hydrocarbons characterizPreparation of alkynesAlkynes are synthesized using both high-temperature industrial methods aChemical properties of alkynesAlkynes are unsaturated hydrocarbons with a single triple bond. Their chArenesArenes, or aromatic hydrocarbons, are a vast class of organic compoundAromaticityAromaticity is a complex of unique structural and chemical features thPreparation and chemical properties of arenesArenes are aromatic hydrocarbons characterized by electrophilic substitElectrophilic substitution in the benzene ringElectrophilic substitution (S_E) is a key mechanism of chemical reactQualitative reactions of alkynesThe qualitative reaction for alkynes using an ammoniacal solution of sSynthesis of higher cycloalkanesTo obtain higher cycloalkanes with a doubled carbon skeleton, intramolDetermining hydrocarbon structure from reaction productsDetermining the structure of an unknown unsaturated hydrocarbon is oft

Frequently asked questions for this section

How to visually distinguish propane cylinders?

Cylinders used for storing and transporting propane are traditionally painted red.

Why doesn't gasoline have a precise boiling point, unlike pure octane?

Because gasoline is a mixture of various alkanes and other hydrocarbons. It is characterized by a boiling range (30–205 °C): as the light fractions evaporate, the boiling point of the remaining liquid in the mixture continuously increases.

Why is it better not to use a mixture of different haloalkanes in the Wurtz reaction?

Because radicals recombine randomly. Instead of a single target substance, you will get a hard-to-separate mixture of three different alkanes (two symmetrical and one asymmetrical).

Why does halogenation slow down when the reaction vessel volume is decreased?

A decrease in volume causes active free radicals to collide with vessel walls more frequently. Their recombination (joining each other) occurs on the walls, causing premature termination of the reaction chain.

Why are alkenes called unsaturated hydrocarbons?

Due to the presence of a double bond in the molecule, they contain a smaller number of hydrogen atoms compared to alkanes with the same carbon skeleton.

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