the angle is 120 degrees.
The formula looks like trans- 2-butene. The c atoms working left to right will have sp3 sp2 sp2, sp3 hybridisation. the bond angles will be tetrahedral on the sp3 centers, 120 0 on the sp2 centres which have a planar shape, with all four substituents lying in the same plane. Good picture in wikipedia. The actual bond angles will deviate slightly.
n+n-n-n-n+n-n-n squared to the 934892547857284579275348975297384579th power times 567896578239657824623786587346378 minus 36757544.545278789789375894789572356757583775389=n solve for n! the answer is 42
n2 + n = n(n + 1)
n^2 + n
its sp2 hybridisation
In pyridine molecule the Nitrogen atom is involved in Aromatic character of ring if lone pair of nitrogen forms a sigma bond with hydrogen the Aromatic ring (Aromaticity) becomes lass stable so pyridine do not accept the proton easily while Aromaticity is not involved in pi-pyridine so its nitrogen atom easily donates the electron pair to a proton .
Pyrrole C4H4NH (in which N contributes a lone pair) has a pKa - 3.8, but Pyridine (where N is part of the ring's double bond) has a pKa 5.14. Electron pair availability indicates the strength of basicity. In this case, pyridine is the stronger base.
sp2
sp2 since the (graphical, with respect to resonance) Lewis structure for NO3- is: one oxygen double bond, the other two is single bond. an electron of N (which have 5 valence e-) is "donated" to O. And an electron gained by the anion is placed on the other O.
The pyridine molecule is a planar and cyclic shape, similar to a regular hexagon. It has a nitrogen atom in the center and five carbon atoms connected to it, forming a ring.
Bases containing the pyridine substructure, or derived from pyridine as a starting material. Pyridine is basically benzene with one of the carbons substituted with a nitrogen, if that helps.
Yes Pyridine is a tertiary amine.
NaCl is not soluble in pyridine.
because pyridine is toxic...so amines are used in place of pyridine.......
pyridine is a base it accept hydrogen and forms pyridine hydrochloride in the synthesis of Aspirin
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