Answer:
See explanation
Explanation:
A. Constitutional or structural isomers have the same molecular formula but different structural formulas.
B. Conformational isomers are compounds having the same atom to atom connectivity but differ by rotation about one or more single bonds.
C. Stereo isomers are compounds having the same molecular mass and atom to atom connectivity but different arrangement of atoms and groups in space.
I. Enantiomers are stereo isomers (optical isomers particularly) that are non-superimposable mirror images of each other.
II. Diasteromers are optical isomers that are not mirror images of each other.
Both diasteromers and enantiomers are types of optical isomers which in turn is one of the types of stereo isomers.
Stereo isomers differ from conformational isomers in that the arrangement of atoms in stereo isomers is permanent while conformational isomers results from free rotations in molecules about single bonds.
Answer:
Electronegativity in group 1 decreases as we go from Lithium to Francium.
Explanation:
Electronegativity is defined as the tendency of an element to attract an electron pair towards itself.
In a group generally this tendency decreases from top to bottom as the size of the atom increases and hence the positive nucleus get far from the outer orbital.
In the same way group 1 elements i.e. from Lithium to Francium electronegativity decreases.
Answer:
Water molecules in the solid state, such as in ice and snow, form weak bonds (called hydrogen bonds) to one another. These ordered arrangements result in the basic symmetrical, hexagonal shape of the snowflake.
Explanation:
