yes
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.
A substituted hydrocarbon created from a hydrocarbon chain is by replacing at least one hydrogen atom with an atom of another element.
True. The chemical properties of substituted hydrocarbons aren't different than the properties of the original hydrocarbons.
Confuguration of allenes: See the links on the left column under edit links.
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>.