Step 1: Understanding chirality
A molecule is chiral if it has at least one chiral center (a carbon attached to four different groups). A molecule is achiral if it lacks chirality, meaning it either has a plane of symmetry or does not have a chiral center.
Step 2: Analyzing each option
(A) 2-bromobutane: The carbon at position 2 is attached to four different groups, making it chiral.
(B) 3-nitropentane: - The carbon at position 3 is bonded to two identical ethyl (\(-{CH}_2{CH}_3\)) groups. - Since it lacks four distinct groups, it is achiral.
(C) 3-chlorobut-1-ene: Has a potential chiral center.
(D) 1-bromoethanol: Contains a chiral carbon due to four different groups. (E) 2-hydroxypropanoic acid: Contains a chiral carbon at position 2.
Step 3: Conclusion The only molecule without a chiral center is 3-nitropentane. Hence, it is the achiral molecule.
For the reaction:
\[ 2A + B \rightarrow 2C + D \]
The following kinetic data were obtained for three different experiments performed at the same temperature:
\[ \begin{array}{|c|c|c|c|} \hline \text{Experiment} & [A]_0 \, (\text{M}) & [B]_0 \, (\text{M}) & \text{Initial rate} \, (\text{M/s}) \\ \hline I & 0.10 & 0.10 & 0.10 \\ II & 0.20 & 0.10 & 0.40 \\ III & 0.20 & 0.20 & 0.40 \\ \hline \end{array} \]
The total order and order in [B] for the reaction are respectively: