Tetrahedral arrangement is resulted upon mixing one s and three p atomic orbitals, resulting in 4 hybridized 
orbitals → hybridization.
<h3>What is
orbital hybridization?</h3>
In the context of valence bond theory, orbital hybridization (or hybridisation) refers to the idea of combining atomic orbitals to create new hybrid orbitals (with energies, forms, etc., distinct from the component atomic orbitals) suited for the pairing of electrons to form chemical bonds.
For instance, the valence-shell s orbital joins with three valence-shell p orbitals to generate four equivalent sp3 mixes that are arranged in a tetrahedral configuration around the carbon atom to connect to four distinct atoms.
Hybrid orbitals are symmetrically arranged in space and are helpful in the explanation of molecular geometry and atomic bonding characteristics. Usually, atomic orbitals with similar energies are combined to form hybrid orbitals.
Learn more about Hybridization
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Answer:
N2
Explanation:
We use the ideal gas equation to calculate the number of moles of the diatomic gas. Then from the number of moles we can get
Given:
P = 2atm
1atm = 101,325pa
2atm = 202,650pa
T = 27 degrees Celsius = 27 + 273.15 = 300.15K
V = 2.2L
R = molar gas constant = 8314.46 L.Pa/molK
PV = nRT
Rearranging n = PV/RT
Substituting these values will yield:
n = (202,650 * 2.2)/(8314.46* 300.15)
n = 0.18 moles
To get the molar mass, we simply divide the mass by the number of moles.
5.1/0.18 = 28.5g/mol
This is the closest to the molar mass of diatomic nitrogen N2.
Hence, the gas is nitrogen gas
The correct answer is A. The image shows a nuclear fission. This takes place in any of the heavy nuclei after capture of a neutron. This is the opposite of nuclear fusion. In this case, nuclei are broken down into two.
Answer and explanation:
cyclopentadiene is more acidic than cyclopentane
hydrocarbon compound are weak acid in nature
This relative acidity is explained by the stability of
cyclopentadienyl anion which is aromatic in nature
(check the attached image file 1)
To answer this question we must look at the stability of the anions that are formed when the compound lose proton.
All the electron in the cyclopentyl anion are localized.
In contrast, the aromatic cyclopentadienyl anion is a stable carbanion as a result of its aromaticity therefore making its conjugate acid a very strong acid compare to other compounds with hydrogen attached to sp³ carbons
