A girl walks \(4km\) towards west,then she walk \(3km\) in a direction \(30°\)east of north and stops.Determine the girls displacement from her initial point to departure.
Let O and B be the initial and final positions of the girl respectively.
Then,the girl's position can be shown as:

Now,we have
\(\overrightarrow{OA}=-4\hat{i}\)
\(\overrightarrow{AB}=\hat{i}|\overrightarrow{AB}|cos60°+\hat{j}|\overrightarrow{AB}|sin 60°\)
\(=\hat{i}3\times\frac{1}{2}+j^{3}\times\frac{\sqrt{3}}{2}\)
\(=\frac{3}{2}\hat{i}+\frac{3\sqrt{3}}{2}\hat{j}\)
By the triangle law of vector addition,we have:
\(\overrightarrow{OB}=\overrightarrow{OA}+\overrightarrow{AB}\)
\(=(-4\hat{i})+(\frac{3}{2}\hat{i}+\frac{3\sqrt{3}}{3}\hat{j})\)
\(=(-4+\frac{3}{2})\hat{i}+\frac{3\sqrt{3}}{2}\hat{j}\)
\(=(-8+\frac{3}{2})\hat{i}+\frac{3\sqrt{3}}{2}\hat{j}\)
\(=\frac{-5}{2}\hat{i}+\frac{3\sqrt{3}}{2}\hat{j}\)
Hence,the girl's displacement from her initial point of departure is
\(\frac{-5}{2}\hat{i}+\frac{3\sqrt{3}}{2}\hat{j}\)
Amines are usually formed from amides, imides, halides, nitro compounds, etc. They exhibit hydrogen bonding which influences their physical properties. In alkyl amines, a combination of electron releasing, steric and H-bonding factors influence the stability of the substituted ammonium cations in protic polar solvents and thus affect the basic nature of amines. Alkyl amines are found to be stronger bases than ammonia. Amines being basic in nature, react with acids to form salts. Aryldiazonium salts, undergo replacement of the diazonium group with a variety of nucleophiles to produce aryl halides, cyanides, phenols and arenes.