Which force prevents protons from repelling each other inside a nucleus?
the gravitational force
the weak nuclear force
the electromagnetic force
<u>the strong nuclear force</u>
<span>a.655 k not 100 percent on this but try it. You will use 273.15 and add your Celcius temp to get it in Kelvin
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Hey, lovely! It's a pretty lengthy process but here is a pretty clear video on how to do it. Hope this helps ya!
https://www.khanacademy.org/science/chemistry/chemical-reactions-stoichiome/balancing-chemical-equat...
Answer:
1) 0.0025 mol/L.s.
2) 0.0025 mol/L.s.
Explanation:
<em>H₂ + Cl₂ → 2HCl.</em>
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<em>The average reaction rate = - Δ[H₂]/Δt = - Δ[Cl₂]/Δt = 1/2 Δ[HCl]/Δt</em>
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<em>1. Calculate the average reaction rate expressed in moles H₂ consumed per liter per second.</em>
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The average reaction rate expressed in moles H₂ consumed per liter per second = - Δ[H₂]/Δt = - (0.02 M - 0.03 M)/(4.0 s) = 0.0025 mol/L.s.
<em>2. Calculate the average reaction rate expressed in moles CI₂ consumed per liter per second.</em>
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The average reaction rate expressed in moles Cl₂ consumed per liter per second = - Δ[Cl₂]/Δt = - (0.04 M - 0.05 M)/(4.0 s) = 0.0025 mol/L.s.
Answer:
The order of reactivity towards electrophilic susbtitution is shown below:
a. anisole > ethylbenzene>benzene>chlorobenzene>nitrobenzene
b. p-cresol>p-xylene>toluene>benzene
c.Phenol>propylbenzene>benzene>benzoic acid
d.p-chloromethylbenzene>p-methylnitrobenzene> 2-chloro-1-methyl-4-nitrobenzene> 1-methyl-2,4-dinitrobenzene
Explanation:
Electron donating groups favor the electrophilic substitution reactions at ortho and para positions of the benzene ring.
For example: -OH, -OCH3, -NH2, Alkyl groups favor electrophilic aromatic substitution in benzene.
The -I (negative inductive effect) groups, electron-withdrawing groups deactivate the benzene ring towards electrophilic aromatic substitution.
Examples: -NO2, -SO3H, halide groups, Carboxylic acid groups, carbonyl gropus.