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Ethylacetate is more polar. IT has a carbonyl group, which means the more electronegative Oxygen is drawing electron density towards oxygen, hence leaves the carbonyl carbon to be delta positive, hence there is polarity between those atoms of the molecule, then there is the ethyl group attached to this same carbonyl carbon, which although there is a degree of induction due to the CH2CH3 somewhat pushing towards the the carbonyl carbon, yet again the oxygen attached draws more density away, than the ethyl aspect pushing in, hence on both fronts, the molecule is polar. NOW in comparison to petroleum ether, well, petroleum ether, is usually short chained alkanes, either pentane, hexane, and is a fraction of refined oil. THE UPPER LIGHTER FRACTION, and not to be compared to say an actual ether, such as diethyl ether. So on that basis, pet ether is non polar. NOW if you meant diethyl ether. ETHYL ACETATE is still more polar, as the ether has one oxygen between methylene groups, or perhaps two methyl groups. and yes, there is an electronegative difference between that oxygen and the carbon next to it, but an ether is flanked by two carbon groups, hence the polarity of the molecule is minimized.

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Q: What is more polar either ethyl acetate or pet ether?
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What is more polar either ethyl-acetate or pet-ether?

on basis of solubility in water. ethyl acetate.


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Is ethyl acetate more polar than toluene?

Yes, ethyl acetate is more polar than toluene.


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Plants material contains Organic compounds along with salts and water, some organic compounds are polar and soluble in ethyl alcohol or ethyl acetate but some are non polar and soluble in ether or hexane, so two types of solvents may be used for plants extraction, the best way is to use non polar solvent first and extract the non polar compounds then use the polar solvent and extract the polar compounds.


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DME (DiMethyl Ether) is rather unpolar because it is symmetrical (+-+), it has a bended or hooked (V-like) structure (about 120o corner) with 'longer, more spread legs' than water (104.5o). It is more polar than di-Ethyl ether however.


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If you'll take a look at its structure benzophenone is polar but during our laboratory we were able to determine if it's polar or non-polar by TLC. The TLC plate was developed in a mixture of petroleum ether and ethyl acetate with a 9:1 ratio respectively. This would mean that the solvent used is non-polar due to the large amount of petroleum ether. Finally our group was able to determine the Rf value of benzophenone and we found out that it has an Rf value of 0.4737 so this would mean that benzophenone is non-polar because its Rf value is near to 1.


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