Structural isomerism is due to the difference in the linkage of atoms or groups without any reference to space

Stereoisomerism is due to the difference in arrangement of atoms or groups in space

Is there any difference in the taste of lemon juice without sugar ?

The isomerism exhibited due to the difference in the size of the alkyl groups attached to the same functional group is

Chain isomerism arises due to difference in the arrangement of carbon atoms constituting the chain

Position isomerism is due to the difference in the position of a functional group, multiple bond or substituent in the same carbon chain

Structural isomers have different covalent linkage of atoms. Stereoisomers are compounds that have same sequence of covalent bonds but differ in the relative dispositions of their atoms in space. Geometri cal and optical isomers are the two important types of configurational isomers. The compound with double bonds or ring structure have restricted rotation, so exist in two geometrical forms. The double bonds in larger rings (ring size 10 carbon large) can also cause geometrical isomerism. The optical isomers rotate the plane of plane-polarised light. A sp^(3) -hybridised carbon atom bearing four different types of substituents is called an asymmetric centre or chiral centre. A chiral object or molecule cannot be superimposed on its mirror image. Stereoisomers that are mirror images of each other are called enantiomers. The stereosomers that the pot mirror images of each other are called diastereomers. Diasteremers have different physical properties. A racemic mixture is optically inactive and contains equal amounts of both the enantiomers. Resolution refers to method of separating a racemic mixture. Into two pure enantiomers. A meso compound is an optically inactive stereoisomer, which is achiral due to the presence of an internal plane of symmetry or centre of symmetry within the molecule. The number of chiral centres present in the following compounds is

Structural isomers have different covalent linkage of atoms. Stereoisomers are compounds that have same sequence of covalent bonds but differ in the relative dispositions of their atoms in space. Geometri cal and optical isomers are the two important types of configurational isomers. The compound with double bonds or ring structure have restricted rotation, so exist in two geometrical forms. The double bonds in larger rings (ring size 10 carbon large) can also cause geometrical isomerism. The optical isomers rotate the plane of plane-polarised light. A sp^(3) -hybridised carbon atom bearing four different types of substituents is called an asymmetric centre or chiral centre. A chiral object or molecule cannot be superimposed on its mirror image. Stereoisomers that are mirror images of each other are called enantiomers. The stereosomers that the pot mirror images of each other are called diastereomers. Diasteremers have different physical properties. A racemic mixture is optically inactive and contains equal amounts of both the enantiomers. Resolution refers to method of separating a racemic mixture. Into two pure enantiomers. A meso compound is an optically inactive stereoisomer, which is achiral due to the presence of an internal plane of symmetry or centre of symmetry within the molecule. The following two compounds are

(A) : Natural rubber and gutta percha are examples of cis-trans isomers. (R) : Cis-trans isomerism arises due to the difference of geometrical arrangement of two different groups on the double bonded carbon atoms.