I don’t have a picture but I can describe it to you.
The hydrogen that is attached at the tertiary position on the heptatriene (at the 7-methyl) would be very acidic, as removal would leave a positive charge that could be moved throughout the ring through resonance. This would mean that the three double bonds would be participating in resonance, and the deprotonated structure would be aromatic, thus making this favorable.
The hydrogen that is attached at the tertiary position on the pentadiene (5-methyl) would NOT be acidic, as removal would cause an antiaromatic structure.
Any other hydrogens would NOT be acidic. Those vinylic to their respective double bonds would seriously destabilize the double bond if removed, and hydrogens attached to the methyl group jutting off the ring have no incentive to leave the carbon.
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Answer:
Light, sound, and waves in the ocean are common examples of waves. Sound and water waves are mechanical waves; meaning, they require a medium to travel through. The medium may be a solid, a liquid, or a gas, and the speed of the wave depends on the material properties of the medium through which it is traveling.
Explanation:
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Answer:
NaNO2 is the formula for sodium nitrite
Explanation:
Check the selected ions chart to find out more in depth.
Answer:
20
step by step explanation:
