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Natalija [7]
3 years ago
14

Help plzz pick on the picture

Chemistry
1 answer:
Oksanka [162]3 years ago
8 0
The answer to this question would most definitely be the last one
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Is it possible to have a bent molecule without a molecular dipole?
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In the context of small molecules with similar molar masses, arrange these intermolecular forces by strength (hydrogen bonding -
Katarina [22]
<h2>Answer:</h2>

Arrangement of inter molecular forces from strongest to weakest.

  • Hydrogen bonding
  • Dipole-dipole interactions
  • London dispersion forces.
<h3>Explanation:</h3>

Intermolecular forces are defined as the attractive forces between two molecules due to some polar sides of molecules. They can be between nonpolar molecules.

Hydrogen bonding is a type of dipole dipole interaction between the positive charge hydrogen ion and the slightly negative pole of a molecule. For example H---O bonding between water molecules.

Dipole dipole interactions are also attractive interactions between the slightly positive head of one molecule and the negative pole of other molecules.

But they are weaker than hydrogen bonding.

London dispersion forces are temporary interactions caused due to electronic dispersion in atoms of two molecules placed together. They are usually in nonpolar molecules like F2, I2. they are weakest interactions.

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Select the reason why two molecules of benzaldehyde cannot react via the aldol condensation.
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Benzaldehyde or C6H5CHO would not undergo the aldol condensation because it does not contain an alpha-hydrogen in its structure. Aldol condensation is a type of reaction that happens between an enolate and an aldehyde or ketone leading to a alkene that has a planar structure. The lack of an alpha-hydrogen would not allow for it to undergo such process since it cannot enolize. Benzaldehyde undergoes a nucleophilic reaction known as Claisen-Schmidt condensation. It has somehow same mechanism of the aldol reaction however, the nucleophilic attack on the carbonyl happens even without the alpha-hydrogen but with an enolate that is from a ketone.
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