The correct option is
D F and G are diastereomers.
Tautomerism is a phenomenon where a single compound tends to exist in two or more structures which are interconvertible and differ in the relative position of one atomic nucleus.
In Keto-enol tautomerism, delocalisation takes place between a >C=O group and an alpha H where the equilibrium lies between a keto form and an enol form.
E, F and E, G are keto enol tautomers.
Geometrical Isomerism arises due to different arrangement of atoms/groups around a system where free rotation of bonds is restricted.
Compound F is cis isomer because similar groups are in same side about the
C−C double bond.
Compound G is trans isomer because similar groups are in opposite side about the
C−C double bond.
Geometrical isomers are diastereomers. Thus, F and G are diastereomers.
E, E and G are not resonance structures.
Hence, correct statements are (b), (c) and (d).