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alkene (unsaturated) vs alkane (saturated) alkyne (unsaturated) vs alkane (saturated) arene (unsaturated) vs cycloalkane (saturated) For organic compounds containing heteroatoms (other than C and H), the list of unsaturated groups is long but some common types are: carbonyl, e.g. ketones, aldehydes, esters, carboxylic acids (unsaturated) vs ...
The formula for acyclic saturated hydrocarbons (i.e., alkanes) is C n H 2n+2. [1]: 623 The most general form of saturated hydrocarbons, (whether linear or branched species, and whether with or without one or more rings) is C n H 2n+2(1-r), where r is the number of rings. Those with exactly one ring are the cycloalkanes.
Aliphatic compounds can be saturated, joined by single bonds (), or unsaturated, with double bonds or triple bonds ().If other elements (heteroatoms) are bound to the carbon chain, the most common being oxygen, nitrogen, sulfur, and chlorine, it is no longer a hydrocarbon, and therefore no longer an aliphatic compound.
Alkanes are found in animal products, although they are less important than unsaturated hydrocarbons. One example is the shark liver oil, which is approximately 14% pristane (2,6,10,14-tetramethylpentadecane, C 19 H 40). They are important as pheromones, chemical messenger materials, on which insects depend for communication.
Bromine test is used to test the saturation of hydrocarbons. [17] The bromine test can also be used as an indication of the degree of unsaturation for unsaturated hydrocarbons. Bromine number is defined as gram of bromine able to react with 100g of product. [18] Similar as hydrogenation, the halogenation of bromine is also depend on the number ...
In organic chemistry, the cycloalkanes (also called naphthenes, but distinct from naphthalene) are the monocyclic saturated hydrocarbons. [1] In other words, a cycloalkane consists only of hydrogen and carbon atoms arranged in a structure containing a single ring (possibly with side chains ), and all of the carbon-carbon bonds are single .
For hydrocarbons, the DBE (or IHD) tells us the number of rings and/or extra bonds in a non-saturated structure, which equals the number of hydrogen pairs that are required to make the structure saturated, simply because joining two elements to form a ring or adding one extra bond (e.g., a single bond changed to a double bond) in a structure reduces the need for two H's.
Steam cracking is a petrochemical process in which saturated hydrocarbons are broken down into smaller, often unsaturated, hydrocarbons. It is the principal industrial method for producing the lighter alkenes (or commonly olefins), including ethene (or ethylene) and propene (or propylene).