Respuesta :
The image of (r)−2−chloropropanoic acid is attached below.
(r)−2−chloropropanoic acid is a mono-basic acid. Further, as compared to propanoic acid it is a strong acid because of -I effect of -Cl atom.
Also, (r)−2−chloropropanoic acid is an optically active compound. It has one chiral centre. Since, the present compound is of r-form, hence it rotates plane polarized light to right.
(r)−2−chloropropanoic acid is a mono-basic acid. Further, as compared to propanoic acid it is a strong acid because of -I effect of -Cl atom.
Also, (r)−2−chloropropanoic acid is an optically active compound. It has one chiral centre. Since, the present compound is of r-form, hence it rotates plane polarized light to right.

Answer:
Image of (R)-2-chloropropanoic acid has been attached below
Explanation:
Here longest carbon chain contain 3 carbon atoms (prop means 3 carbon).
Functional group is -COOH (suffix oic acid means presence of -COOH group in longest carbon chain)
Numbering should start by assigning (1) to carbon in -COOH group
One stereocenter present at (2) position.
According to CIP rule of assigning preference to substituents in a stereocenter, Cl(a), -COOH (b), -Me(c) and H(d).
Cl should remain above the plane and H below the plane so that [tex](a)\rightarrow (b)\rightarrow (c)[/tex] gives clockwise rotation keeping (d) far apart from viewing side.
