I cannot find an exact figure for acetamide but it should be strongly polar due to its functional groups (amine and C=O). Also, dimethyl acetamide is 6.5 polarity (polar and the extra CH3 groups should make DM acetamide less polar than acetamide).
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Yes, acetaminophen is a polar molecule due to its hydroxyl group that creates partial positive and negative charges. This polarity allows acetaminophen to be water-soluble and easily absorbed in the body.
yes if you test on a TLC you will find that the substans do not follow the front like a unpolar substanse would
Acetaminophen is polar due to the presence of hydroxyl (OH) and amide (CONH2) groups in its structure. These functional groups result in uneven distribution of electron density within the molecule, making it polar.
The order of increasing polarity for these substances is: caffeine < ibuprofen < acetaminophen < aspirin. Caffeine is the least polar, whereas aspirin is the most polar among these common pain relievers.
Phenacetin will have a higher Rf value than acetaminophen in a TLC separation on silica gel using a non-polar developing solvent. This is because phenacetin is more non-polar than acetaminophen, causing it to move further up the TLC plate and have a higher Rf value.
Acetaminophen is most soluble in polar solvents like water, methanol, and ethanol. It is not very soluble in nonpolar solvents like hexane or chloroform.
No, acetaminophen is not conductive in water. Acetaminophen is an organic compound that does not dissociate into ions in water, thus it does not conduct electricity.