is the orbital hybridization of a central atom that has one lone pair and bonds to three other atoms.
<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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C. Tripling the length and reducing the radius by a factor of 2 is the change to a pipe would increase the conductance by a factor of 12.
<u>Explanation:</u>
As we know that the resistance is directly proportional to the length of the pipe and it is inversely proportional to the cross sectional area of the pipe.
So it is represented as,
R∝ l /A [ area is radius square]
So k is the proportionality constant used.
R = kl/A
Conductance is the inverse of resistance, so it is given as,
C= 1/R.
R₁ = kl₁ / A₁
R₂ = kl₂/A₂
R₂/R₁ = 1/12 [∵ conductance is the inverse of resistance]
= l₂A₁ / l₁A₂
If we chose l₁/l₂= 3 and A₂/A₁= 4 So R₂/R₁= 1/3×4 = 1/12
So tripling the length and reducing the radius by a factor of 2 would increase the conductance by a factor of 12.
Lowery-Bronsted theory is applied here. Acc. to this theory Base accepts protons and Acids donate proton.
Part 1:
Aniline is less basic than ethylamine because the lone pair on nitrogen (which accepts proton) is not localized. It resonates throughout the conjugated system of phenyl ring. Hence due to unavailability of electrons for accepting proton it is less basic compare to ethylamine. In ethyl amine the lone pair of electron is localized and available to abstract proton.
Part 2:
In this case the alkyl groups attached to -NH₂ (in ethylamine) and -O⁻ (in ethoxide are same (i.e. CH₃-CH₂-). Ethoxide is more basic than ethylamine because ethoxide is a conjugate base of ethanol (pKa value of ethanol = 15.9 very weak acid) and the conjugate base of weak acid is always a strong base. Secondly, the oxygen atom more Electronegative than Nitrogen atom can attract more electron cloud from alkyl group as compared to Nitrogen in ethylamine. Hence, oxygen in ethoxide attains greater electron cloud than the nitrogen in ethylamine. Therefore, it is more basic than ethylamine.
I think the correct answer from the choices listed above is the first option. The Greeks were the first to use the term atom. In 450 BCE, Democritus coined the term átomos which means "uncuttable" or "the smallest indivisible particle of matter".
