Despite the large difference in electronegativity between #"Si"# and #"F"#, #"SiF"_4# has a boiling point lower than that of #"NH"_3# (#-86^@ "C"#, vs. #-33^@ "C"#). Why is that? Could it be due to the symmetry? Hydrogen-bonding?
Note: the #"Si"-"F"# bond length is #"155.4 pm"# , and the #"N"-"H"# bond length is #"101.2 pm"# .
Note: the
There are two answers
1.) Because of the hydrogen bonds (precisely interactions)
2.) Because of the tetrahedral arrangement of Si-F
Though the large difference in electronegativity between
This is because that boiling is completely dependent on intermolecular forces and not on intramolecular forces.
And in
Because that London Dispersion Forces are temporary because electron density is always changing all across the atom dipole-dipole forces are much stronger because they are permanent and always in alignment.
Despite the large difference in electronegativity between
And more stronger the intermolecular force more the boiling point
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The difference in boiling points between silicon tetrafluoride (SiF4) and ammonia (NH3) can be attributed to several factors. While the electronegativity difference between silicon (Si) and fluorine (F) is significant, other factors such as molecular weight and molecular geometry also play a role. In the case of SiF4, its larger molecular weight contributes to stronger van der Waals forces, which can increase its boiling point compared to NH3. Additionally, the molecular geometry of SiF4 is tetrahedral, leading to weaker intermolecular forces compared to the more polar and asymmetric NH3 molecule, which can also affect the boiling point. Hydrogen bonding, a significant factor in NH3, is not present in SiF4 due to the absence of hydrogen atoms. Therefore, while electronegativity differences are important, other molecular properties also influence the boiling points of compounds.
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When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
- What are three types of Van der Waals forces?
- Do only non-polar molecules experience London dispersion forces?
- How do water molecules act like "little magnets"?
- Where, and how does hydrogen-bonding occur? Does such bonding occur in #HCF_3#?
- What type of molecule has dipole-dipole interactions and what type has London dispersion forces?

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