How do the chemical properties of oxides change from left to right across a period? From top to bottom within a particular group
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Aniline can be produced from nitro-benzene by reduction. When nitro-benzene reacts with tin (Sn) + hydrochloride acid (HCl) then aniline is produced. The Sn + HCl forms free hydrogen ions which converts the nitro group of the benzene ring to amine group, which is aniline. In place of Sn + HCl. One can use palladium (Pd) hydrogen mixture in presence of ethanol (EtOH). There produces a side product in this reaction which is cyclohexyl amine. The reaction can be shown as.
Structure of a-chloro-b-methylbutyric acid (2-chloro-3-methylbutyric acid is attached below.
The structure was drawn using following information.
1) First, the parent chain was identified. The parent chain is containing four carbon atoms, also, this chain belongs to carboxylic acid as the compound name ends with Butyric acid i.e. butyr (Butane) -ic acid (carboxylic acid).
2) Secondly, the positions of substituents were assigned by using the rule which sates that the numbering in carboxylic acid must satrt from the carbonyl carbon. Therefore, the carbon which is attached to carbonyl carbon is named as alpha (2nd position) and carbon next to alpha carbon is named as beta carbon (3rd position). Hence, we add chlorine atom on 2nd carbon next to carbonyl group and methyl group at 3rd carbon with respect to carbonyl carbon.
