[PDF] Naming Ethers and Thiols (Naming and Properties) PDF Naming-Ethers-and-Thiols-Naming-and-Properties.pdf

Cyclic ethers (heterocyclic compounds) are often given common names DO NOT memorize IUPAC Names for Ethers The shorter alkyl group and the oxygen are

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Ethers

• Contain an ─O─ between two carbon groups. • That are simple are named by listing the alkyl names in alphabetical order followed by ether Cyclic ethers (heterocyclic compounds) are often given common names. DO NOT memorize!

IUPAC Names for Ethers

The shorter alkyl group and the oxygen are named as an alkoxy group attached to the longer hydrocarbon.

methoxy propane CH 3 - O - CH 2 - CH 2 - CH 3

1 2 3

Numbering the longer alkane gives: 1-methoxypropane

Treat all R-O- groups that you find in a molecule as alkoxy groups or branches (substituents), and follow the previous

rules we've covered for all other families.

Properties of Ethers

• Slightly polar. • Cannot be H-bond donors. • Are H-bond acceptors (soluble in water up to 4 C's). • Simple ethers are highly flammable (many form explosive peroxides).

Anesthetics

• Inhibit pain signals to the brain. • Such as ethyl ether CH 3 ─CH 2 ─O─CH 2 ─CH 3 were used for over a century, but caused nausea and were flammable. • Developed by 1960s were nonflammable. Cl F F Cl F H H─C─C─O─C─H H─C─C─O─C─H F F F H F H

Ethane(enflurane) Penthrane

Methyl tert-butyl ether (MTBE)

• Is one of the most produced organic chemicals. • Is a fuel additive used to improve gasoline combustion. • Use is questioned since the discovery that MTBE has contaminated water supplies.

Reyes Free to copy for educational purposes

Thiols

Thiols or mercaptans, are sulfur analogs of alcohols. (The -SH group is called the mercapto, or sulfhydryl group.)

The IUPAC nomenclature system adds the ending -thiol to the name of the alkane, but without dropping the final -e.

• Often have strong odors. • Are used to detect gas leaks. • Are found in onions, oysters, garlic and skunk.

Physical Properties

Thiols have considerably lower boiling points than those of alcohols, even though thiols have higher molecular masses,

because thiols do not possess the strong hydrogen bonding of alcohols. • Thiols (R-SH) react with mild oxidizing agents to yield a disulfide (R-S-S-R). • easily reduced back to thiols

Disulfides are named by naming the R groups attached to the sulfur atoms followed by the word disulfide.

Many proteins contain thiol groups and disulfides critical to maintaining their three dimensional shape and their proper

functioning.

Lead and mercury salts react with thiol groups, altering the physiological functioning of the proteins involved.

A common source of lead is from flakes of paint manufactured prior to 1980. The use of lead tetraethyl as a gasoline

additive also introduces lead into the environment, however its use has been phased out.

Mercury from insecticides and other sources enters the food chain through fish from contaminated rivers, lakes, and

streams. Mercury has a physiological effect similar to that of lead. Reyesquotesdbs_dbs10.pdfusesText_16

[PDF] [PDF] Naming Ethers and Thiols (Naming and Properties)