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<h2><em><u>Technically yes but no because you have to fill the 3s orbital before the 5s orbital</u></em></h2>
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2-bromo-3,4-dimethylpentane is combined with t-butoxide. The product of this reaction is 3,4 dimethyl - 1- pentene.
The reaction of 2-bromo-3,4-dimethylpentane is combined with t-butoxide forms 2 alkene in the elimination reaction due to steric hindrance. The least stable alkene 3,4 dimethyl - 1- pentene is easy to make. the t-butoxide is (CH₃)₃CO⁻. The reaction involves in this reaction is E2 elimination reaction. This reaction involves the one step reaction. The product will also form that is 3,4 dimethyl - 2 - pentene. so the reaction involve Elimination reaction and the product due to steric hindrance is 3,4 dimethyl - 1- pentene
Thus, 2-bromo-3,4-dimethylpentane is combined with t-butoxide. The product of this reaction is 3,4 dimethyl - 1- pentene.
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Hydrogen-1, Carbon-13, Nitrogen-15, Fluorine-19, and Phosphorus-31 are the most useful. Out of these, Hydrogen-1 and Carbon-13 in NMR are the most useful nuclei because the these atoms are the most commonly present in organic molecules.
Three complete orders on each side of the m=0 order can be produced in addition to the m = 0 order.
The ruling separation is
d=1 / (470mm −1) = 2.1×10⁻³ mm
Diffraction lines occur at angles θ such that dsinθ=mλ, where λ is the wavelength and m is an integer.
Notice that for a given order, the line associated with a long wavelength is produced at a greater angle than the line associated with a shorter wavelength.
We take λ to be the longest wavelength in the visible spectrum (538nm) and find the greatest integer value of m such that θ is less than 90°.
That is, find the greatest integer value of m for which mλ<d.
since d / λ = 538×10⁻⁹m / 2.1×10 −6 m ≈ 3
that value is m=3.
There are three complete orders on each side of the m=0 order.
The second and third orders overlap.
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