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What are the angles between sp2 orbitals?
the angle is 120 degrees.
What is the shape bond angle and hybridization of CH3CH double bond CHCH3?
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.
What is the hardest math question ever?
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
Adding n to the second power to n?
n2 + n = n(n + 1)
If my number is n then n x n x n x n equals 625 what is my number?
n = 5
What is the hybridization of the nitrogen atom of pyridine?
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.
What is the hybridization of pyridine?
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.
Is pyridine deet?
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.
Why pyrrole is more acidic and less basic than pyrrolidine?
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.
Why pyridine is less basic than piperidine?
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.
What is the hybridization of the central atom in NOBr?
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.
What is the products when pyridine reacts with sodamide and pyrrolidine?
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.
What is the hybridization of the orbitals around the n atom in HNO2?
sp2
What type of shape is the pyridine?
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.
What is the products obtained when pyridine reacts with sodamide?
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.
Is pyridine is a tertiary amine?
Yes Pyridine is a tertiary amine.
Can sodium chloride be solved in pyridine?
NaCl is not soluble in pyridine.
