Yes, it is chiral
No, there are no chiral centres.
This is a single bonded compound and cis-trans isomerism is only possible when fre rotation about a bond is restricted or a double bond or cycle is essential for existence of cis-trans isomers.
those are defined by position of double bonds, the possible one,s are cis-cis,cis-trans,trans-trans.
Cis and trans are configuration.
cis
Yes: cis-3-hexene and trans-3-hexene.
No. When bromine (aq) reacts with cyclohexene, the compound is now saturated, and will no longer have C=C bonds, thus it is unable to exhibit cis-trans isomerism.
All molecules in a "pure" compound are made up of the same atoms in the same order in structure with the same bonds. Sometimes there are subtle differences such as double bonds that can be either U shaped (CIS) or Z shaped (Trans). Or even a right-handed or left-handed orientation of atoms in a molecule (Chiral).
Cis and trans compounds are isomers of one another, the difference being in the position of the hydrogen atoms attached to the two carbons forming a double bond in an unsaturated hydrocarbon chain. If the hydrogen atoms in both carbons are on the same side then it causes a kink in the change and is called cis, whereas if the hydrogen atoms are on opposite sides then the chain is straight and is called trans (the convention is to write both these words in italics). So the terms cis or trans tell you the shape of the hydrocarbon chain in a compound.
The cis-trans isomerism tend to be very stable. Typically, trans isomers are more stable however, an exception lies in cis-trans isomers which makes them more stable than trans isomers.
Opposite of latin `trans` is `cis`
Cis and trans refers to the different faces of a Golgi complex. Vesicles come into the cis face from the ER and leave from the trans face to the plasma membrane or Lysosomes.