Answer by Raman P
If a compound contains a C atom that is attached to 4 different atoms or groups, then it will be 'optically active' & have optical isomers. The simplest example is lactic acid- CH3- CH(OH)CO2H- the 4 groups /atoms make it have a laevo rotatory, & dextro rotatory isomers, which are mirror images - identical, but not super imposable, & hence asymmetric .More about this can be had from a good organic chemistry text. Coming to the compds: peroxyacetic acid & ethanol are not optically active . Fructose is a keto hexose : a sugar containing six C atoms , & a ketone group. It has five asymmetric C atoms, & hence can have 2*5 optical isomers[ plus several other aldohexose isomers like glucose. Nature is symmetrically asymmetric, in a sense . that is why we have the different DNA/RNA combinations ,......
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