Boiling point of ethanol is higher than its isomer methane due to the presence of hydrogen bond in ethanol
The R(-)-isomer of adrenaline is more potent. Its orientation allows its benzylic hydroyxl to form a hydrogen bond with Serine410 whereas this doesn't happen with S(-)-isomers of adrenaline.
No, because it has 2 fewer hydrogen atom than propane Propane=C3H8 Cyclopropane =C3H6
Regardless of the isomer dichlorobenzene will have 12 atoms in total: 6 carbon, 4 hydrogen, and 2 chlorine.
No. CaCl2 is neither ans isomer, nor does it have isomers.
Ethanol has no structural isomer because of its short chain
C2H6 and isomer would have the same simple chemical formula. In the case of this molecule though, an isomer is not possible.
Yes. Ethanol is a structural isomer of dimethyl ether. CH3OCH3.
Yes it is. It's structural isomer is ethanol C2H5OH
Because , Cis isomer are same group on same side of the c=c bond . & those are bulky group on the same side , they are formed steric repulsion to each other then Cis isomer are less stable than trans isomer is same group of opposite side of c=c bond no formation of steric repulsion to each other. and trans isomer is more stable than Cis isomer.....
An isomer shares the same number of the same atoms, but they are configured differently.
No, it is NOT either both. Besides 'benzenepropanol' is not an official name.
If you mean what is an isomer then it is a compound with the same chemical formula but with a different structure
the ortho isomer is more acidic because the carboxylate anion (the conjugate base) can be stabilized through hydrogen-bonding.
Isomer is the term used for chemical compounds having the same molecular formula, in physics the term isomer is meaningless although the term Isotope is used.
methoxy methane is a functional group isomer of ethanol. CH3-O-CH3
yes, it is functional isomer of diethyl ether and methylpropyl ether.
Ammonia (NH3) hasn't an isomer.The solution of ammonia in water is called ammonium hydroxide.
Z isomer are cis isomer it has the tow groups at the same side around the double bond but the E isomer are trance isomer it has the tow groups at opposite side around the double bond.
The "CO" refers to the carboxyl, the "R" refers to the alkyl and the "N" refers to the nitrogen. Look at the carbon chiral atom of the carbohydrate with the hydrogen atom behind. If CO-R-N is clockwise, then it is a D isomer. If CO-R-N is anti-clockwise, then it is a L isomer.