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: 16.32 g of as excess reagent are left.
Explanation:
To calculate the moles :
According to stoichiometry :
2 moles of require = 1 mole of
Thus 0.34 moles of will require=
of
Thus is the limiting reagent as it limits the formation of product and
is the excess reagent.
Moles of left = (0.68-0.17) mol = 0.51 mol
Mass of
Thus 16.32 g of as excess reagent are left.