# Comparing the basicity of benzamide and acetamide

What if we were asked to compare the basicity of benzamide and acetamide?

Which one of them would be more basic? I read somewhere on the internet that benzamide must be more basic than acetamide due to cross conjugation (I am not aware of this term). Is this true? Please provide an explanation.

• For starters, do you know which atom will get protonated? Then one needs to think what stabilisation resulting cation will have. Even if you get to solution with inductive and mesomeric effects which may satisfy someone who'd ask you it still may be not consistent with other effects and, more importantly, experimental results, so it's more of a mind game. – Mithoron Aug 4 '18 at 22:44

Where do amides accept protons?

As Mithoron aptly pointed out in the comments, it is first important to establish which atom in the amide molecule receives the proton. Due to the strong delocalisation present in the amide, the nitrogen lone pair becomes very weakly basic and it is the lone pair on the carbonyl oxygen which is donated to form bonds with $$\ce {H^+}$$. Not only does the delocalisation diminish the basicity of the nitrogen lone pair, the donation of the lone pair from the nitrogen atom towards the carbonyl group effectively raises the energy of the lone pairs present on the oxygen atom.

This is more clearly illustrated in the molecular orbital picture, where we consider the interactions between the lone pair orbital on $$\ce {N}$$ and the $$\ce {C=O}$$ $$\pi$$ and $$\pi^*$$ MOs. The interaction with the $$\pi$$ MO helps to increase the energies of the electrons on the $$\ce {O}$$ atom while the interaction with the $$\pi^*$$ MO helps to lower the energy of the lone pair on the $$\ce {N}$$.

Let's look at some data

I personally find that a theoretical approach to this problem without looking at any data is non-trivial and may potentially give a false conclusion since many factors are at play. In fact, my initial thoughts without looking at any data was that benzamide would be more basic since the benzene ring can donate into the $$\ce {C=O}$$ group via resonance (in the same way as how a benzyl carbocation is stabilised by the donation of $$\pi$$ electrons from the ring) and this would certainly enhance the basicity of the carbonyl oxygen since the electron density at the oxygen atom would have increased significantly.

Cox et al. (1980) have determined via empirical measurements the $$\ce {pk_a}$$s of the conjugate acids of acetamide and benzamide to be $$\ce {-0.73}$$ and $$\ce {-1.54}$$ respectively, with an uncertainty of $$\ce {0.02}$$. This tells us that acetamide is actually more basic than benzamide. In the discussion of their results, the authors considered the factors which they thought underlied this basicity difference. These included the following:

• Effect 1: inductive withdrawal due to the more electronegative $$\ce {sp^2}$$ hybridised carbon atoms of the aromatic ring, decreasing basicity of benzamide
• Effect 2: resonance stabilisation of the positive charge in the conjugate acid of the benzamide molecule, increasing the basicity of benzamide
• Effect 3: more negative entropy change of ionisation for benzamide, decreasing basicity of benzamide

The authors suggested that perhaps, effects 1 and 3 were more significant combined than effect 2, resulting in the observed difference. Effect 3 was not well-explained by the authors. I suppose effect 3 arises due to the difference in size of the methyl and phenyl substituents and the consequent difference in the extent of their solvation. The conjugate acid of benzamide may require more solvation and hence, a greater ordering of water molecules, giving rise to a more negative entropy change. This is my rationalisation of effect 3.

Further insights provided

In addition to determining the acidity constants of the conjugate acids, the authors also calculated the deviation from coplanarity of the the benzene ring of the various N-substituted benzamides. They observed that as the deviation from coplanarity increased due to the presence of large and bulky substituents on the $$\ce {N}$$ atom, the $$\ce {pk_a}$$ value of the N-substituted benzamides became more "acetamide-like". They then went on to say:

This shows that whatever the nature of the effect which causes benzamide to be less basic than acetamide, the degree of coplanarity in the molecule is important to it.

Perhaps, there is intramolecular hydrogen bonding?

I believe that the effect at play here that was not mentioned by Cox et al. may be the presence of intramolecular hydrogen bonding in the benzamide molecule. To highlight the significance of this effect, I will now discuss the computational findings of Muthuraja et al. (2017). The following image (the grahical abstract of their study) shows the subject of the computation study and it also shows the computed Mulliken charges on the different atoms. Notice that most of the aromatic $$\ce {H}$$s have much more signficant positive charge (i.e. in excess of $$\ce {+0.1}$$ compared to the other protons not bound to the aromatic ring. Additionally, note the large negative charge value on the carbonyl oxygens.

The authors posit high possibility of intramolecular hydrogen bonding between the carbonyl oxygen of the lactam with the neighbouring aromatic proton. They cite the following evidence justifying their claim:

• Firstly, the $$\ce {O...H}$$ distance ($$\ce {2.18}$$ angstroms) is shorter than their van der Waal distance ($$\ce {2.72}$$ angstroms)
• Secondly, the carbonyl stretching frequency is red-shifted from the normal stretching frequency

From this computation study, I simply wish to point out that there is a significant chance that intramolecular hydrogen bonding may be present in benzamide due to the proximity of the carbonyl oxygen to the aromatic proton. This interaction decreases the availability of the lone pair on the carbonyl oxygen for donation to acids. Thus, benzamide is less basic. Furthermore, this agrees with the additional insight provided by Cox et al. (1980): As deviation from coplanarity increases, there is less and less intramolecular $$\ce {H}$$ bonding and thus, greater and greater availability of the lone pairs on the $$\ce {O}$$ for donation to acids.

References

1. Cox, R. A.; Druet, L. M.; Klausner, A. E.; Modro, T. A.; Wan, P.; Yates, K. Protonation acidity constants for some benzamides, acetamides, and lactams. Can. J. Chem 1980, 59, 1568-1573.

2. Muthuraja, P.; Shanmugavadivua, T.; Joselin Beaulab, T.; Bena Jothy, V.; Dhandapani, M. Influence of intramolecular hydrogen bonding interaction on the molecular properties of N-p-tolyl-5-oxo pyrrolidine-3-carboxylic acid: A theoretical and experimental study. Chem. Phys. Lett. 2017, 691, 114-121.