When 2,4-hexadiene is protonated, a resonance-stabilized secondary allylic carbocation is formed. Draw the curved arrow notation
below that shows the movement of electrons between the two major resonance structures.
1 answer:
Answer:see the image for the structure of the allylic carbocation
Explanation:
When 2,4-hexanediene is protonated at the 5-position as shown in the image, a carbonation is formed which can be stabilized by resonance. The positive charge can be found on carbon 4 or carbon 2 due to resonance of the allylic carbonation. The both structures are shown and electron movements were depicted using curved arrow notation in the structures shown in the image attached.
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Answer:-
Explanations:- The solution we have is a buffer solution and we know that a buffer solution resists a change in its pH if a strong acid or base is added to it.
Here, the buffer solution we have is of a weak base and it's conjugate acid. So, a strong acid(nitric acid) is added to this buffer then it reacts with the base present in the buffer so that the acid could be neutralized. This is called buffer action.
The net ionic equation is written as:
Note that is a strong acid and nitrate ion is the spectator ion so it is not included in the net ionic equation.
%Mass
Ar C = 12 g/mol, Mr C₄H₁₀ = 58 g/mol, Ar H = 1 g/mol
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