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Explain Cyclobutane
Cyclobutane undergoes an interconversion of puckered forms analogous to the chair interconversion of cyclohexane. This interchanges axial and equatorial groups. Thus, one conformation of trans1,2-dimethylcyclobutane-the more stable conformation-has diequatorial substituents, and the other-the less stable conformation-has diaxial substituents
Chemical Kinetics of the Peroxodisulfate Ion The peroxodisulfate ion is one of the strongest oxidants that are called, although the oxidation reaction is relatively slow.
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Rutherford's α particle scattering experiment proved that atom has: (1) Electrons (2 )Neutron (3) Nucleus (4 )Orbitals Ans: Nucleus
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