Why does $\ce{NH4Cl}$ form an ionic bond if the difference in electronegativity between nitrogen and chlorine is $0$?
Shouldn't it be at least 1.7 in order for an ionic bond to form? If not what is the reason behind this?
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Sign up to join this communityWhy does $\ce{NH4Cl}$ form an ionic bond if the difference in electronegativity between nitrogen and chlorine is $0$?
Shouldn't it be at least 1.7 in order for an ionic bond to form? If not what is the reason behind this?
Explicit valence of $\ce{N}$ is four, $\ce{N}$ of $\ce{NH4+}$ cannot form another (covalent) bond with $\ce{Cl-}$.
The chemistry of $\ce{NH4+}$, owing to similar size, charge, and polarizing power, is similar to that of alkali metal ions, especially $\ce{K+}$; $\ce{NH4+Cl-}$ is ionic just like $\ce{K+Cl-}$ is, with about $\pu{80\%}$ ionic character.
The gap between HOMO of $\ce{Cl-}$ and LUMO of $\ce{NH4+}$ is about $\pu{5 eV}$ making any covalent interaction rather weak; $\ce{NH4+}$ doesn't have available empty orbitals to make a covalent bond with $\ce{Cl-}$.
It is commonly known that $\ce{N}$ does not form more than four bonds. A similar question (How many bonds can nitrogen form?) on chemistry stack exchange answered this. Since, $\ce{N}$ in $\ce{NH4+}$ forms four bonds with four $H$, another covalent bond is not possible; moreover, it is forming a complete octet, which is especially stable for elements with atomic number $Z \leq 10$.
$\ce{NH4+}$, due to its size and charge, as you mentioned, often shows similarity to alkali metal ions, especially $\ce{K+}$. By this analogy, since alkali metals for ionic bonds with halides, so does the $\ce{NH4^+}$ cation.
According to reference$^1$
(Thus,) the room-temperature $\ce{NH4+Cl-}$ bond length estimated from equation (5) is $\pu{3.28} \overset{\circ}{\text{A}}$ , corresponding to the $r_\ce{NH4+}$ value of $\pu{1.47} \overset{\circ}{\text{A}}$.
Comparing with values given in reference$^2$, this value falls within the (Pauling) ionic radii of $\ce{K+}$ ($\pu{1.33} \overset{\circ}{\text{A}}$) and $\ce{Rb+}$ ($\pu{1.48} \overset{\circ}{\text{A}}$). Also note the Gourary and Adrian Electron-density (ionic) radius of $\ce{K+}$ is $\pu{1.49} \overset{\circ}{\text{A}}$.$^2$. Thus, $r_\text{ionic}(\ce{NH4+}) \approx r_\text{ionic}(\ce{K+}), r_\text{ionic}(\ce{Rb+})$.
Especially in Biochemistry, chemistry of $\ce{NH4+}$ has often been compared with that of $\ce{K+}$. For example, in reference$^3$, it is stated:
(We conclude) that a unique transporter, a potassium-ammonium ($\ce{K+}$/$\ce{NH4+}$) antiport, is responsible for $\ce{NH4+}$ transport in renal inner medullary collecting duct cells. This antiporter is sensitive to verapamil and Schering 28080, is electroneutral, and is selective for $\ce{NH4+}$ and $\ce{K+}$ as substrates. The $\ce{K+}$/$\ce{NH4+}$ antiporter may play a significant role in acid-base regulation by excretion of ammonium and elimination of acid.
Citing reference$^3$, it is stated in reference$^4$
Since host–guest chemistry may also include non-metallic cations, it is interesting to note that the K+ ion has been stated to be similar to the ammonium ion ($\ce{NH4+}$).
Furthermore, as calculated by MolCalc, the difference between the HOMO of $\ce{Cl-}$ and LUMO of $\ce{NH4+}$, both lying at energies greater than zero ( $\pu{2.73 eV}$ for $\ce{Cl-}$ and $\pu{7.21 eV}$ for $\ce{NH4+}$), is about $\pu{5 eV}$, making any covalent interaction rather weak (not occurring in this case).
On the effective ionic radii for ammonium. Sidey, V. (2016). Acta Cryst. B72, 626-633. 10.1107/S2052520616008064
Conway, B.E., Ayranci, E. Effective Ionic Radii and Hydration Volumes for Evaluation of Solution Properties and Ionic Adsorption. Journal of Solution Chemistry 28, 163–192 (1999). 10.1023/A:1021702230117
Hassane Amlal, Manoocher Soleimani, K+/NH4+ antiporter: a unique ammonium carrying transporter in the kidney inner medulla, Biochimica et Biophysica Acta (BBA) - Biomembranes, Volume 1323, Issue 2, 1997, Pages 319-333, ISSN 0005-2736, 10.1016/S0005-2736(96)00200-3
Kim, Y., Nguyen, TT.T., Churchill, D.G. (2016). Bioinorganic Chemistry of the Alkali Metal Ions. In: Sigel, A., Sigel, H., Sigel, R. (eds) The Alkali Metal Ions: Their Role for Life. Metal Ions in Life Sciences, vol 16. Springer, Cham. 10.1007/978-3-319-21756-7_1
As there is no bond between nitrogen and chlorine in ammonium chloride, it cannot be either ionic either covalent. Nitrogen bonding in an ammonium cation is fully saturated by four covalent bonds to four hydrogen atoms.
It has the same symmetry but with opposite charges as potassium perchlorate. There is no bond between potassium and chlorine either.
Think of it this way. Electronegativity is defined as the tendency of an atom to pull electrons towards itself. So, say you have an atom having a positive charge, it will obviously having more power to pull electrons towards itself.
Having a difference of 1.7 is not something applying everywhere. There are ionic compounds with difference less than that.
This value defined to $1.7$ is an order of magnitude, valid for about $50$% of all the bonds. It does not prevent ionic bonds existing between $\ce{N}$ (in the center of $\ce{NH4^+}$) and $\ce{Cl^-}$.