Answer:
The strongest force that exists between molecules of Ammonia is <em>Hydrogen Bonding</em>.
Explanation:
Hydrogen Bond Interactions are those interactions which are formed between a partial positive hydrogen atom bonded directly to most electronegative atoms (i.e. F, O and N) of one molecule interacts with the partial negative most electronegative atom of another molecule.
Hence, in ammonia the nitrogen atom being more electronegative element than Hydrogen will be having partial negative charge and making the hydrogen atom partial positive. Therefore, the attraction between these partials charges will be the main force of interaction between ammonia molecules.
Other than Hydrogen bonding interactions ammonia will also experience dipole-dipole attraction and London dispersion forces.
Answer:
chlorine and I think maybe sulphur. but check the internet
Answer:
[He]: 2s² 2p⁵.
[Ne]: 3s².
[Ar]: 4s² 3d¹⁰ 4p².
[Kr]: 5s² 4d¹⁰ 5p⁵.
[Xe]: 6s² 4f¹⁴ 5d¹⁰ 6p².
Explanation:
- Noble elements are used as blocks in writing the electronic configuration of other elements as they are stable elements.
He contains 2 electrons fill 1s (1s²).
So, [He] can be written before the electronic configuration of 2s² 2p⁵.
Ne contains 10 electrons fill (1s² 2s² 2p⁶).
So, [Ne] can be written before the electronic configuration of 3s².
Ar contains 18 electrons is configured as ([Ne] 3s² 3p⁶).
So, [Ar] can be written before the electronic configuration of 4s² 3d¹⁰ 4p².
Kr contains 36 electrons is configured as ([Ar] 4s² 3d¹⁰ 4p⁶).
So, [Kr] can be written before the electronic configuration of 5s² 4d¹⁰ 5p⁵.
Xe contains 54 electrons is configured as ([Kr] 5s² 4d¹⁰ 5p⁶).
So, [Xe] can be written before the electronic configuration of 6s² 4f¹⁴ 5d¹⁰ 6p².
Answer:
Option A - High frequency, short wavelength.
Explanation:
<em>If the sound is high then the frequency is also high but short-wavelength means lots of waves that always have a high pitch-sound and a high frequency. </em>
Answer:
Four substitution products are obtained. The carbocation that forms can react with either nucleophile (H2O or CH3OH) from either the top or bottom side of the molecule
Explanation:
An SN1 reaction usually involves the formation of a carbocation in the slow rate determining step. This carbocation is now attacked by a nucleophile in a subsequent fast step to give the desired product.
However, the product is obtained as a racemic mixture because the nucleophile may attack from the top or bottom of the carbocation hence both attacks are equally probable.
The attacking nucleophile in this case may be water or CH3OH
