All the atoms in a conjugated system are _. The fewer electrons involved in the conjugated system, the energy gap between HOMO and LUMO will be _. and therefore the wavelength of the photon involved in the absorption process will be _. Being the energy of the HOMO _ than LUMO's, the process of absorption will take place when an electron goes from _. Considering the molecule on the left, there are _ carbon atoms forming a conjugated system. The picture on the right _ a resonance form of the picture on the left.

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Chapter1: Chemical Foundations
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All the atoms in a conjugated system are _. The fewer electrons involved in the conjugated system, the energy gap between HOMO and LUMO will be _. and therefore the wavelength of the photon involved in the absorption process will be _. Being the energy of the HOMO _ than LUMO's, the process of absorption will take place when an electron goes from _.

Considering the molecule on the left, there are _ carbon atoms forming a conjugated system. The picture on the right _ a resonance form of the picture on the left.

The image depicts two chemical structures involving aromatic rings and aliphatic substituents.

**Left Structure:**
- The structure consists of a benzene ring, which is characterized by a six-membered carbon ring with alternating double bonds, indicating aromaticity.
- Attached to the benzene ring is a vinyl group (–CH=CH₂) via a single bond, where the second carbon atom in the vinyl group has a methyl group (–CH₃) bonded to it. This forms an isopropenyl group attached to the benzene ring.

**Right Structure:**
- This structure also contains a benzene ring with alternating double bonds, showing its aromatic nature.
- Attached to the benzene ring is a positively charged vinyl group (the carbon closest to the ring is positively charged, denoted by a plus sign).
- The benzene ring has a negative charge, indicated by a minus sign inside a circle.

These chemical structures illustrate the concept of resonance and charge distribution in organic chemistry, showcasing how substituents can alter electron density and stability in aromatic systems.
Transcribed Image Text:The image depicts two chemical structures involving aromatic rings and aliphatic substituents. **Left Structure:** - The structure consists of a benzene ring, which is characterized by a six-membered carbon ring with alternating double bonds, indicating aromaticity. - Attached to the benzene ring is a vinyl group (–CH=CH₂) via a single bond, where the second carbon atom in the vinyl group has a methyl group (–CH₃) bonded to it. This forms an isopropenyl group attached to the benzene ring. **Right Structure:** - This structure also contains a benzene ring with alternating double bonds, showing its aromatic nature. - Attached to the benzene ring is a positively charged vinyl group (the carbon closest to the ring is positively charged, denoted by a plus sign). - The benzene ring has a negative charge, indicated by a minus sign inside a circle. These chemical structures illustrate the concept of resonance and charge distribution in organic chemistry, showcasing how substituents can alter electron density and stability in aromatic systems.
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