Why Are These Ring Structures Considered Diastereomers?

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NY152
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Please post this type of questions in HW section using the template.
Could someone explain to me why the ring structures in this photo are diastereomers? From looking at them, I see a plane of symmetry, and no chiral centers so I'm unsure how they're diastereomers without have R/S characteristics
 
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  • Homework problem 11 with four structures: two pairs of Fischer-style and wedge-dash compounds labeled with R/S assignments, plus two cyclohexane ring structures each with a methyl and an ethyl substituent drawn with wedge and dash bonds.
    Screen Shot 2017-03-14 at 1.10.51 PM.png
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They are cis-trans or geometrical isomers. I believe these days geometrical isomers are classified as a subset of diastereomers. Chiral atoms are not necessary for diastereoisomerism.