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.
You might be interested in
Answer:
Approximately 75%.
Explanation:
Look up the relative atomic mass of Ca on a modern periodic table:
- Ca: 40.078.
There are one mole of Ca atoms in each mole of CaCO₃ formula unit.
- The mass of one mole of CaCO₃ is the same as the molar mass of this compound:
.
- The mass of one mole of Ca atoms is (numerically) the same as the relative atomic mass of this element:
.
Calculate the mass ratio of Ca in a pure sample of CaCO₃:
.
Let the mass of the sample be 100 g. This sample of CaCO₃ contains 30% Ca by mass. In that 100 grams of this sample, there would be of Ca atoms. Assuming that the impurity does not contain any Ca. In other words, all these Ca atoms belong to CaCO₃. Apply the ratio
:
.
In other words, by these assumptions, 100 grams of this sample would contain 75 grams of CaCO₃. The percentage mass of CaCO₃ in this sample would thus be equal to:
.
Answer:
2.01atm
Explanation:
