This is because it has 3 double bonds, it has 6 cis- trans isomer and since it has functional group of carboxylic acid which contains a double bond due to which there is 2 more isomers..Total = 8...Draw the structural formula to be more clear.
Tartaric acid has three stereoisomers: meso-tartaric acid and the two enantiomers, D-tartaric acid and L-tartaric acid.
Three
Tartaric acid has two chiral centers, leading to a total of four possible stereoisomers. Therefore, there are three stereoisomers for the L-tartaric acid form and one for the D-tartaric acid form.
Three isomers of C2HfClBr are possible.
C3H4O can have two isomers: propynal and cyclopropanone.
Tartaric acid has three stereoisomers: meso-tartaric acid and the two enantiomers, D-tartaric acid and L-tartaric acid.
Three
Nonane has a total of 75 isomers, which includes straight chain isomers, branched chain isomers, and cyclic isomers.
Tartaric acid has two chiral centers, leading to a total of four possible stereoisomers. Therefore, there are three stereoisomers for the L-tartaric acid form and one for the D-tartaric acid form.
Three isomers of C2HfClBr are possible.
C3H4O can have two isomers: propynal and cyclopropanone.
There are two isomers for dibromopropane: 1,2-dibromopropane and 2,2-dibromopropane.
There are a total of three structural isomers of C7H16 that have no secondary hydrogen atoms. These isomers are 2-methylhexane, 3-methylhexane, and 2,2-dimethylpentane.
Three
C6H8O7 is the formula for citric acid. This is stuff like pure lemon juice and pure orange juice.
This compound (dibromomethane) has only one form. It does not form isomers .
None, as it has 5 structural isomers in which none of are optically active.