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
The nitrogen atom of pyridine is sp2 hybridized. It participates in the aromatic ring system of pyridine and forms three sigma bonds with neighboring carbon atoms, resulting in the sp2 hybridization.
The hybridization of the nitrogen atom in pyridine is sp2. This is because the nitrogen is bonded to three other atoms, resulting in a trigonal planar geometry.
No, pyridine is not the same as DEET. Pyridine is a basic heterocyclic organic compound, while DEET (N,N-diethyl-meta-toluamide) is a common active ingredient in insect repellents.
Pyrrole is more acidic than pyrrolidine because the nitrogen lone pair in pyrrole is part of the aromatic ring, making it less available for protonation. Pyrrolidine is less acidic and more basic than pyrrole because the nitrogen lone pair is not part of an aromatic system, allowing it to readily accept a proton.
Pyridine is less basic than piperidine because the nitrogen in pyridine is part of an aromatic ring, which delocalizes the lone pair of electrons on the nitrogen atom and makes it less available for proton donation. In contrast, piperidine has a more localized lone pair on the nitrogen atom, making it more readily available for proton donation, thus making piperidine a stronger base than pyridine.
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.
When pyridine reacts with sodamide (NaNH2) and pyrrolidine, it forms a C-N bond cleavage product by replacing the nitrogen atom of the pyridine ring with the amide group from sodamide. The resulting product is a pyridine with an amide group attached to its carbon atom.
sp2
The pyridine has six points and is in the shape of a hexagon. The pyridine is an organic compound with the chemical formula C5 H5 N and occurs in many compounds.
When pyridine reacts with sodamide, the products obtained are sodamide anion (NaNH2) and a protonated pyridine molecule. The NaNH2 acts as a strong base and abstracts a proton from the pyridine molecule to form sodamide anion and a protonated pyridine.
Yes Pyridine is a tertiary amine.
NaCl is not soluble in pyridine.