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  2. Zeisel determination - Wikipedia

    en.wikipedia.org/wiki/Zeisel_determination

    The ensuing reaction results in the cleavage of the ether or the ester into an alkyl iodide and respectively an alcohol or a carboxylic acid. Zeisel determination. By heating this mixture, the gases are allowed to come into contact with a piece of paper higher up the test tube saturated with silver nitrate.

  3. Ether - Wikipedia

    en.wikipedia.org/wiki/Ether

    In organic chemistry, ethers are a class of compounds that contain an ether group—a single oxygen atom bonded to two separate carbon atoms, each part of an organyl group (e.g., alkyl or aryl). They have the general formula R−O−R′ , where R and R′ represent the organyl groups.

  4. Diol - Wikipedia

    en.wikipedia.org/wiki/Diol

    Provided that there are enough carbon atoms that the angle strain is not too much, a cyclic ether can be formed. A common diol reaction to produce a cyclic ether. 1,2-diols and 1,3-diols can be protected using a protecting group. [13] Protecting groups are used so that the functional group does not react to future reactions.

  5. Demethylation - Wikipedia

    en.wikipedia.org/wiki/Demethylation

    Demethylation often refers to cleavage of ethers, especially aryl ethers. [12]Historically, aryl methyl ethers, including natural products such as codeine (O-methylmorphine), have been demethylated by heating the substance in molten pyridine hydrochloride (melting point 144 °C (291 °F)) at 180 to 220 °C (356 to 428 °F), sometimes with excess hydrogen chloride, in a process known as the ...

  6. List of chemistry mnemonics - Wikipedia

    en.wikipedia.org/wiki/List_of_chemistry_mnemonics

    A mnemonic is a memory aid used to improve long-term memory and make the process of consolidation easier. Many chemistry aspects, rules, names of compounds, sequences of elements, their reactivity, etc., can be easily and efficiently memorized with the help of mnemonics.

  7. Ether cleavage - Wikipedia

    en.wikipedia.org/wiki/Ether_cleavage

    Ether cleavage refers to chemical substitution reactions that lead to the cleavage of ethers. Due to the high chemical stability of ethers, the cleavage of the C-O bond is uncommon in the absence of specialized reagents or under extreme conditions. [1] [2] In organic chemistry, ether cleavage is an acid catalyzed nucleophilic substitution reaction.

  8. Glossary of chemistry terms - Wikipedia

    en.wikipedia.org/wiki/Glossary_of_chemistry_terms

    This glossary of chemistry terms is a list of terms and definitions relevant to chemistry, including chemical laws, diagrams and formulae, laboratory tools, glassware, and equipment. Chemistry is a physical science concerned with the composition, structure, and properties of matter , as well as the changes it undergoes during chemical reactions ...

  9. Glycerophospholipid - Wikipedia

    en.wikipedia.org/wiki/Glycerophospholipid

    The first carbon of glycerol has a hydrocarbon chain attached via an ether, not ester, linkage. The linkages are more resistant to chemical attack than ester linkages are. The second (central) carbon atom has a fatty acid linked by an ester. The third carbon links to an ethanolamine or choline by means of a phosphate ester.