It's shaped like an X....now place the substituents in any order you choose. You will see that either a cis or trans isomer also exists.
The second question is most easily understood by applying the concept of resonance. Because the pi electrons are delocalized...each double bond has "less" double bond character than that of ethene where the pi electron is localized to a greater extent.
why would the bonds between SiO2 be closest to 110
when Kaplan says that CO2 is 180 degrees apart, and dont Si and C both have sp hybridization because they both have 4 valence electrons
why would the bonds between SiO2 be closest to 110
when Kaplan says that CO2 is 180 degrees apart, and dont Si and C both have sp hybridization because they both have 4 valence electrons