UV-1 || Basic principle of UV-visible spectroscopy || Electronic transitions || UV spectroscopy

UV-2 || Forbidden, Not Allowed & Allowed Transitions || UV-visible spectroscopy

UV-3 || Why Broad bands in UV-visible spectroscopy || UV-visible spectroscopy

UV-4 || Single beam spectrophotometer | Sources, monochromator & detectors | UV-visible spectroscopy

UV-5 || Double beam UV-visible spectrophotometer || Instrumentation || UV-visible spectroscopy

UV-6 || Common Solvents in UV-visible spectroscopy || Effect of solvent on n-π* and π-π* transitions

UV-7 || Chromophore in UV-visible spectroscopy || n-σ* & n-𝛑* transitions || 𝛑-𝛑* transitions

UV-8 || Auxochrome || UV-Visible spectroscopy || How auxochromes intensified colour?

UV-9 || Bathochromic, hypsochromic, hyperchromic & hypochromic shifts || UV-Visible spectroscopy

UV-10 || Effect of conjugation on ʎmax & εmax || UV-Visible spectroscopy || Intensity of absorption

UV-11 || Effect of pH on ʎmax & εmax in UV-visible spectroscopy || Chromophore & auxochrome

UV-12 || Woodward-Fieser rules for Calculation of ʎmax of dienes || UV-visible spectroscopy

UV-13 || Woodward-Fieser Rules || UV-Visible spectroscopy || Exocyclic double bonds

UV-14 || Woodward-Fieser rules for enones || Exocyclic bonds || UV-visible spectroscopy

UV-15 || Woodward-Fieser Rules for aldehydes, carboxylic acids & esters || UV-visible spectroscopy

UV-16 || Types of absorption bands in UV-visible spectroscopy || Formation of K, R, B and E bands

UV-17 || Absorption bands in benzene || Molecular orbitals of benzene || UV bands of aromatic system

UV-18 || Woodward-Fieser rules for aromatic compounds || UV-Visible spectroscopy

UV-19 || Effect of substituents on ʎmax & εmax of aromatic systems || UV-visible spectroscopy

UV-20 || ʎmax & εmax of polycyclic aromatic hydrocarbons |UV-visible spectroscopy

UV-21 || Effect of steric hindrance & coplanarity on ʎmax & εmax || UV-visible spectroscopy

UV-22 || How to interpret UV-visible spectra? || How to solve UV-visible spectra?