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Chemistry Articles

Difference Between Phenol, Phenyl, Benzene, Benzyl, and Aryl

It is easy to identify the simplest aromatic hydrocarbon Benzene that is made of only two atoms- Carbon and hydrogen. Benzene is a planar, cyclic ring molecule with six sides. It has an alternating double bond that contributes to its extra stability by endowing it with resonance, a phenomenon of electron delocalization.  The molecular formula of Benzene is C6H6 and the structure is-

What are haloalkanes and haloarenes? How can they be classified?

A Haloalkane is the Halogen derivative of an alkane obtained by replacing of one or more hydrogen atoms.

For example, when one Hydrogen of an alkane, Methane, is replaced with a Halogen, for instance, Chlorine, the haloalkane obtained is chloromethane.

                                                               Alkane                 Haloalkane

What is Degree/Level of Unsaturation (LU) or Double Bond Equivalent (DBE)? How to find and interpret DBE values?

Pre-requisite Reading: Identifying single bond, double bond, triple bond, saturation, and unsaturation. 

The DBE calculation uses the general molecular formula to find the presence of unsaturation in a compound. The unsaturation is calculated in levels or degrees. The lowest degree of unsaturation (DOU) indicates minimum unsaturation; there is the least loss of hydrogens to form pie bonds or cyclic rings like in cycloalkanes.

What are s-block elements?

If all the elements were to create a gated community for themselves; they would build four apartment blocks namely, the s-block, p-block, d-block and the f-block. The elements having similar property would be grouped together occupying one block and this behavior is based on the orbital the last electron chooses to enter.

Types of Equivalent Hydrogens (structurally and chemically similar)

The Hydrogens attached to a Carbon atom are said to be equivalent if they are in a same chemical environment. Same chemical environment means that under a reaction condition, these hydrogens would lose their identities of being attached to separate Carbons and behave like an identical set. 

Identifying such hydrogen types would help in predicting the number of monohalogen products that could be obtained on free radical halogenation reaction