Can You Give Two Examples Each Of Organic And Inorganic Compounds

The Strunz classification includes a class for organic minerals. A polymer ˈ p ɒ l ɪ m ər.

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There do not exist any particular collection of rules for writing the trivial naming of compounds.

Can you give two examples each of organic and inorganic compounds. These examples are simple ones in which the molecules easily fit into one class predominantly. An example of an ambident nucleophile is the thiocyanate ion which has the chemical formula of SCN. Polymers range from familiar synthetic plastics such as polystyrene to.

Examples of this include phenol acetic acid and toluene. The Trivial Nomenclature system involves a non-systematic approach to the naming of organic compounds. Organic chemistry calls these categories Functional Groups.

Greek poly- many -mer part is a substance or material consisting of very large molecules or macromolecules composed of many repeating subunits. Names of organic compounds are simplified via this system. For example whewellite CaC 2 O 4 H 2 O is an oxalate that can be deposited in hydrothermal ore veins.

Due to their broad spectrum of properties both synthetic and natural polymers play essential and ubiquitous roles in everyday life. More complex molecules may belong to many categories. While hydrated calcium oxalate can be found in coal seams and other sedimentary deposits.

A Nucleophile which can execute nucleophilic attacks from two or more different places in the molecule or ion is called an Ambident Nucleophile. Ether any of a class of organic compounds characterized by an oxygen atom bonded to two alkyl or aryl groups. These rare compounds contain organic carbon but can be formed by a geologic process.

Attacks from these types of nucleophiles can often result in the formation of more than one product. Ethers are similar in structure to alcohols and both ethers and alcohols are similar in structure to waterIn an alcohol one hydrogen atom of a water molecule is replaced by an alkyl group whereas in an ether both hydrogen atoms are replaced by alkyl or aryl groups. The ability to predict synthetic outcomes then begins and ends with identifying functional groups within a compounds structure.

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