Trimethyl methanol is another name for t-butanol, so I will refer to it as such to avoid confusion. It's easier to think about this problem in terms of their conjugate bases. Methyl groups are more electron donating than hydrogen atoms. So in t-butoxide, the O- has more electron density than the O- in methoxide. More electron density means the t-butoxide "wants" a proton more. In other words, t-butanol "wants" to keep its proton more than methanol does. This makes t-butanol a weaker acid (with a higher pKa), since the stronger acid is the one that loses its proton more readily.
Methyl alcohol (methanol) is actually not the most acidic compound. Stronger acids, such as hydrochloric acid (HCl) or sulfuric acid (H2SO4), have lower pKa values and are more acidic than methanol. Methanol is a weak acid compared to these stronger acids.
Because acetic acid have methyl group ,a electron donating group
For the same reason that water isn't a gas. Oxygen is highly electronegative and the hydrogen bonding present in water and methanol raises the intermolecular attractive forces and results in a higher boiling point.
salicylic acid (an acid) is more polar than methyl salicylate (an ester)
3-methyl butanoic acid is more acidic than butanoic acid because the presence of the methyl group in 3-methyl butanoic acid increases the electron-withdrawing effect, making the molecule more acidic by stabilizing the conjugate base.
HCO3 (bicarbonate) is weaker than HNO3 (nitric acid). Bicarbonate is a weak acid, while nitric acid is a strong acid. This means that nitric acid completely ionizes in water, while bicarbonate only partially ionizes.
acetic acid is vinegar!
Methyl stearate is a saturated fatty acid methyl ester, while methyl oleate is an unsaturated fatty acid methyl ester. Methyl oleate has a higher degree of unsaturation due to a double bond in its carbon chain, making it more flexible and less rigid than methyl stearate. Additionally, methyl oleate may have different physical properties, such as a lower melting point, compared to methyl stearate.
Actually, benzoic acid is the stronger acid when compared to ethanoic acid. This is due to the delocalisation of the lone pair of electrons on the oxygen atom into the benzene, increasing the polarity of the -OH bond and thus makes the cleaving of the H+ ion easier. The delocalisation of electrons into the benzene ring also stabilises the carboxylate ion. Therefore the position of equilibrium lies more to the right and this shows that benzoic is a more acidic acid. The simplified version is that a benzene ring is electron withdrawing and a methyl group is electron releasing. The electron withdrawing power makes the releasing of the H+ ion easier.
Benzoic acid is the stronger acid compared to ethanoic acid. However, ethanoic acid is more corrosive and will burn skin etc more than benzoic acid. Corrosivity/burn potential are not the same as acid strength. This is due to the delocalisation of the lone pair of electrons on the oxygen atom into the benzene, increasing the polarity of the -OH bond and thus makes the cleaving of the H+ ion easier. The delocalisation of electrons into the benzene ring also stabilises the carboxylate ion. Therefore the position of equilibrium lies more to the right and this shows that benzoic is a more acidic acid. The simplified version is that a benzene ring is electron withdrawing and a methyl group is electron releasing. The electron withdrawing power makes the releasing of the H+ ion easier.
HBr is a weaker acid than HCl because the bond between hydrogen and bromine is longer and weaker than the bond between hydrogen and chlorine. This makes it easier for HCl to release its hydrogen ion in solution, making it a stronger acid compared to HBr.
Isopropyl alcohol (isopropanol), the alcohol found in rubbing alcohol, is slightly better at killing bacteria than ethyl alcohol for E. coli and the bacteria in MRSA. Methyl alcohol, or methanol, is the weakest medical alcohol in terms of killing bacteria.