yes
Yes, substituted allenes can exhibit stereoisomerism. This is because the double bonds and substituents around the allene carbon atoms can create different spatial arrangements leading to geometric isomers, also known as E-Z isomers.
Because covalent bond is rigid and occurs in any direction.Because of its ability to orient in any spatial arrangement in space it exhibits stereo-isomerism which is also the property of stereo-isomerism.
Allenes are optically active.
If a carbon atom forms four covalent bonds with four different atoms or groups, the particular carbon is said to be chiral. And the molecule shows stereoisomerism around that atom.
True. The chemical properties of substituted hydrocarbons aren't different than the properties of the original hydrocarbons.
True. The chemical properties of substituted hydrocarbons aren't different than the properties of the original hydrocarbons.
Absolute configuration of allenes is determined by the Cahn-Ingold-Prelog (CIP) priority rules, where the highest priority group is assigned to the highest atomic number attached to the central carbon. If the highest priority groups on both ends point in the same direction, it is R-configuration, and if they point in opposite directions, it is S-configuration. Rotating the molecule to align the priorities correctly can help determine the absolute configuration of allenes.
Because covalent bond is rigid and occurs in any direction.Because of its ability to orient in any spatial arrangement in space it exhibits stereo-isomerism which is also the property of stereo-isomerism.
Allenes are optically active.
A useful rule for the specifying of absolute configuration of allenes alkylidenecycloalkanes and other organic complex systems The Noroozi Rule is useful method for the specifying of absolute configuration of allenes, spiranes, alkylidenecycloalkanes, hexahelicenes, biphenyles and trans-cyclooctenes. see URL: chem.sci.utsunomiya-u.ac.jp/v9n1/noroozi/noroozi.pdf
touluene All Biphenyls and Allenes are optically active without a chiral center
Stereoisomerism is a type of isomerism were the atoms that are in the molecules are the same and there arrangement are the same but there spatial arrangements are different to eachother.
The isomers can be separated by a method called stereoisomerism. The first person that is documented to have used this method is one Louis Pasteur.
4 syllables in substituted.
the substituted hitter gets the at bat
Alcohol
The past tense of "substitute" is "substituted."
Evaluation at x = <whatever value was substituted>.