muscarine has three stereocenters (aka chirality centers) therefore:
2^3=8
in conclusion, muscarine can have 8 stereoisomers.
provided it has a tetrahedral geometry
Your question is not specific enough - what do you mean by isomer? If you mean stereoisomers (likely question with biomolecules) the two most common stereoisomers of glucose are L-glucose and D-glucose. There are 4 chiral carbons in glucose so there would be 42 or 16 possible stereoisomers. The other most important stereoisomers would be mannose and galactose.
The ring form has 8 enantiomers, the open form 4.
In cranberrys..
Stereoisomers are isomeric molecules that have the exact same molecular formula, but a different three dimensional position. A conformer is a set of stereoisomers.
There are 5 chirality centers, so there are 5^2 (=25) stereoisomers.
provided it has a tetrahedral geometry
what do this mean stereoisomers mean
there are 128 stereoisomers of cholesteol . from the formula 2^n where n is the total number of chiral centers. As for cholesterol, there are 8 stereocenters therefore 2^8= 128
Your question is not specific enough - what do you mean by isomer? If you mean stereoisomers (likely question with biomolecules) the two most common stereoisomers of glucose are L-glucose and D-glucose. There are 4 chiral carbons in glucose so there would be 42 or 16 possible stereoisomers. The other most important stereoisomers would be mannose and galactose.
No it is not. There are no stereoisomers
The Thalidomide tragedy was caused in part by a lack of knowledge of stereochemistry. One of the stereoisomers was toxic the other was not.
The ring form has 8 enantiomers, the open form 4.
Agonist is muscarine and antagonist is atropine.
An antimuscarinic is a drug which disrupts the action of muscarine on the nervous system.
In cranberrys..
Stereoisomers are isomeric molecules that have the exact same molecular formula, but a different three dimensional position. A conformer is a set of stereoisomers.