Noun:

নাবালকত্ব,

nonane's Usage Examples:

This is the list of structural isomers of nonane.

{{Area_{octane}} \over {Area_{nonane}}}={{k_{octane}\times M_{octane}\times V_{octane}} \over {k_{nonane}\times M_{nonane}\times V_{nonane}}}} Since both compounds.

1]nonane or 9-BBN is an organoborane compound.

Tedisamil (3,7-dicyclopropylmethyl-9,9-tetramethylene-3,7-diazabicyclo-3,3,1-nonane) is an experimental class III antiarrhythmic agent currently being investigated.

Tetradecane 5-(1-Ethylpropyl)nonane 3-Ethyl-4-(1-methylpropyl)octane 4-(1-Ethylpropyl)-2-methyloctane.

reaction nonane-4,6-dione + H2O ⇌ {\displaystyle \rightleftharpoons } pentan-2-one + butanoate Thus, the two substrates of this enzyme are nonane-4,6-dione.

Where there is enough oxygen, nonane burns to form water and carbon dioxide, so 2-methyloctane would do the same.

2]nonane (TC-1698), a novel alpha7 ligand, is prevented through angiotensin II activation.

It is one of the isomers of nonane.

Decane 2-Methylnonane 3-Methylnonane 4-Methylnonane 5-Methylnonane 3-Ethyloctane 4-Ethyloctane 4-n-Propylheptane.

5-Butylnonane 5-(1-Methylpropyl)nonane (or 5-sec-Butylnonane) 5-(2-Methylpropyl)nonane (or 5-Isobutylnonane) 4-(1,1-Dimethylethyl)nonane (or 4-tert-Butylnonane).

1]nonane-2,6-dione".

An example of Karasch addition is the synthesis of 1,1,3-trichloro-n-nonane from 1-octene, chloroform and [[ferric chloride](FeCl2)].

2]nonane rearrangement product, the original synthesis had to be modified as follows;.

Undecane 3-Ethylnonane 4-Ethylnonane 5-Ethylnonane 4-Propyloctane 4-(1-Methylethyl)octane or 4-isopropyloctane.

1]nonane, commonly known as 9-BBN, a reagent in organic chemistry used in hydroborations:.

1]nonane" in Encyclopedia of Reagents for Organic Synthesis 2001 John Wiley, New.

5-Ethyldecane 4-Propylnonane 5-Propylnonane 4-(1-Methylethyl)nonane 5-(1-Methylethyl)nonane 4-(1,1-Dimethylethyl)octane or 4-tert-Butyloctane 3-Ethyl-4-propylheptane.