Organic Chemistry Practice Problems and Problem Sets
amine bases
Rank the amines A through D below in order of decreasing basicity (1 = most basic). Explain your reasoning.
sp2 carbons are more electronegative (electron withdrawing) than sp3 carbons due to increased s-character. Electron withdrawing groups (EWG) make acids more acidic and bases less basic.
For this reason, piperidine (compound A) is the more basic than pyridine (compound B):
(more basic) A > B (less basic)
Nitro (-NO2) is an EWG, so 4-nitropyridine (compound C) will be less basic than compound A.
Dimethylamine is an electron donating group (EDG), so it adds electron density to pyridine and increases basicity. So dimethylamino pyridine (DMAP, compound D) will be more basic than compound A:
(more basic) D > B > C (less basic)
So how does compound A compare with compound D? There is no way of predicting this based on EWG/EDG rules alone. After all, what should be more basic: piperidine, which has sp3 carbons (increases base strength), or DMAP, which has sp2 carbons (decreases base strength) but also an EDG (increases base strength) ?
There's no way to tell. But it turns out that Piperidine is a little more basic than DMAP. So the overal order is:
(more basic) A > D > B > C (least basic)
MendelSet practice problem # 752 submitted by Matt on July 27, 2011.
Imidazole (shown below) has two nitrogen atoms, N-1 and N-3. Which nitrogen is more basic?
To answer this problem, draw the product after each nitrogen protonates, and compare their stabilities. Explain your reasoning.
Imidazole is aromatic. When N-3 protonates, the product is still aromatic.
But when N-1 protonates, the product is no longer aromatic (and therefore significantly less stable).
Because of this, N-3 is much more basic than N-1. Another way of thinking of this is that the lone pair on N-1 is involved in the aromatic circuit, and so is not available to pick up a proton.
MendelSet practice problem # 584 submitted by Matt on July 9, 2011.