What is the Iupac name of the following crown ether?

1,4,7,10,13,16-Hexaoxacyclooctadecane

PubChem CID	28557
Chemical Safety	Laboratory Chemical Safety Summary (LCSS) Datasheet
Molecular Formula	C12H24O6
Synonyms	18-Crown-6 17455-13-9 1,4,7,10,13,16-HEXAOXACYCLOOCTADECANE 18-Crown-6 ether 18-crown-6-ether More…
Molecular Weight	264.31

What is crown ether in organic chemistry?

A “crown ether ” is a cyclic ether containing several (i.e., 4, 5, 6 or more) oxygen atoms. It is possible to dissolve ionic compounds in organic solvents using crown ethers.

What is crown ether and Cryptates?

Crown ethers are cyclic polyethers that define two-dimensional intramolecular cavities, while cryptands are nitrogenous macrocyclic compounds that define three-dimensional intramolecular cavities. Cite.

How do you name Cryptand?

The most common and most important cryptand is N[CH2CH2OCH2CH2OCH2CH2]3N; the systematic IUPAC name for this compound is 1,10-diaza-4,7,13,16,21,24-hexaoxabicyclo[8.8. 8]hexacosane.

Are ethers polar?

The C – O bonds in ether are polar and thus ethers have a net dipole moment. The weak polarity of ethers do not appreciably affect their boiling points which are comparable to those of the alkenes of comparable molecular mass. Ethers have much lower boiling points as compared to isomeric alcohols.

What is the difference between crown ether and cryptand?

Crown ethers are cyclic polyethers that define two-dimensional intramolecular cavities, while cryptands are nitrogenous macrocyclic compounds that define three-dimensional intramolecular cavities.

What are Spherands?

Spherands are molecules that were designed to include a cation within a ‘spherical’ array of Lewis basic donor groups.