Explanation:
this is your answer hope it will help you
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.
Hope this helps!
Answer:
their warfare had changed dramatically
We will need to see what the picture looks like post the picture of the molecule
Answer:
Ethyl acetate is a polar solvent.
Explanation:
As you can see, the image below shows the chemical formula of Ethyl acetate. This compound has two oxygen atoms, whose electronegativity is greater than that of the carbon atom to which they are attached, the dipole moment of this molecule is nonzero. This phenomenon causes this compound to form dipole-dipole bonds with other polar molecules. This also means that polar compounds can dissolve in Ethyl acetate.