Answer:
The net ionic equation is
H₃O⁺+NH₃ ↔ NH₄⁺+H₂O
Explanation:
To write the net ionic equation, we are required to dissociate the into ions all strong acids and strong bases
Hence, nitric acid which is a strong acid is dissociated as follows
HNO₃+H₂O → H₃O⁺ + NO₃⁻
in the above equation, the nitrate ion NO₃⁻, is a spectator ion because it is only present and does not partake in the chemical reaction so it is left out of the net ionic equation equation
Also the it is required to keep together weak bases in the solution therefore for NH₃ which is a weak base we have
NH₃ + H₃O⁺ → NH₄⁺ + H₂O
Hence, the net ionic equation becomes
H₃O⁺ (aq) + NH₃ ↔ NH₄⁺(aq) + H₂O (l)
6.79 x 10⁶
<h3>Further explanation </h3>
Scientific Notation consists of 2 parts
1. the first part: the first digit followed by the decimal point
2. The second part: the power of 10 (the exponents).which shows the number of digits after the decimal point
To add/subtract, the exponents must be the same and then add/subtract the coefficient
- convert the largest exponent
- subtract the coefficients
4 carbon chain is butane. With a triple bond it is butane. Since the triple bond is on the first carbon it can be called 1-butyne, or but-1-yne.
In resonance structures, the chemical connectivity in the molecule is same but the distribution of electrons are different around the structure. They are created by moving electrons in double or triple bonds, and not atoms.
Phenol, 
and methanol, 
both are alcohols that contain an 
group attached to carbon atom.
Due to loss of 1 
from phenol, it forms phenoxide anion and due to presence of double bond in the benzene ring the negative charge on the oxygen atom (which represents electrons) will resonate with double bonds of benzene ring as shown in the image. The resonance-stabilized phenoxide ion is more stable. Whereas when methanol lose 1 it forms methoxide anion and there are no such electrons present in the structure of methoxide that will result in the movement of electron. Since, due to resonance-stabilized phenoxide ion is more stable than methoxide ion, so it is a stronger acid.
The structures of the anions resulting from loss of 1 from phenol and methanol is shown in the image.
