All Questions
Tagged with stereochemistry chirality
135
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Why is α-truxillic acid not meso compound? [duplicate]
I know that for a compound to be meso it should be optically inactive and should have multiple chiral centres but in case of α-truxillic acid, it is optically inactive due to centre of symmetry being ...
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Optical rotation and chirality
I had the same question as in Molecular chirality and optical rotation
In the answer, it says that there can't be such a mirror position where the effect of one molecule be cancelled by other. But I'm ...
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Which enantiomer of 3-Chloro-2-pentanol is this?
I think that there is a chiral centers at $C_2$ and at $C_3$ (Numbering starting such that the carbon with hydroxy attached is number 2.
Then, for $C_2$:
Priority would be: OH > $C_3$ > $C_1$ &...
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Why the C4 in this 1,3,4,5-substituted Cyclohexanes has a R/S configuration?
(1S,3S,4S,5S)-3,5-dimethoxy-1-phenylcyclohexane-1,4-dithiol.
ChemDraw21 shows the C4 is S configuration. However I think C4 has two same function groups(C3 and C5 are both S configuration; C2-1-6 and ...
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Doubt in chirality and pseudo chirality
So a carbon atom is chiral if it has 4 different group attached to it, and it is pseudo chiral if it has 3 different groups of atoms attached to it, where the 2 similar groups have different ...
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To what extent should a question such as: "how many enantiomers are there?" take geometric isomerism into account?
Pretty simple question here.
How many enantiomers are there for the structure $\ce{CH3CH=CHCH(CH3)CH2CH3}$?
On the one hand, there is just one chiral centre so one would suggest $2$. On the other ...
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Why is Carbon marked as 1 acting like a pseudo chiral centre?
Since there is a plane of symmetry passing through the middle of the compound, the C (chiral centres) at 2 and 3 will rotate the light through angles opposite in magnitude, say, +A and -A respectively ...
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Assigning configuration of chiral plane - selecting of the pilot atom
I am little confused about when it comes to assigning configuration of planarly chiral cyclophanes - and I think it comes down to selection of pilot atom.
All sources I have came across say that the ...
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Can we always use the planar representation of cycloalkanes instead of their true conformations to study their stereochemistry and chirality?
When I have drawn stereoisomers of substituted cyclohexanes and checked if they are chiral, I typically represent the ring as a planar hexagon and look for symmetry elements. For example, I would use ...
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Which one has higher priority in CIP rules -- O or OH?
I know that if the atom is the same, I have to look at the next atom. In the first choice, Oxygen is not connected to any other atom (besides the chiral carbon). It is an anion. Whereas in the second ...
- 135
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Does norcamphor have enantiomers?
The following two molecular structures have two chiral centers, so in total four chiral centers:
I did the absolute configuration multiple times and I keep getting R,R and S,S, which should be ...
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How can a molecule with a double bond on one side have a plane of symmetry, and thus, be achiral?
Does norbornene have a plane of symmetry? Is norbornene achiral or chiral?
I think norbornene is chiral since there is a double bond on the only one side. Thus, there is no plane of symmetry. The ...
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Why does 2,3 dichlorobutane have 2, and not 3, stereoisomers
I understand how and that the R,S and R,R stereoisomers are different.
But I don’t see why the R,R and S,S compounds are stereoisomers and not meso compounds with each other.
Online it says that ...
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Is There a Problem with the Assignment of Stereochemical Descriptors by ChemDraw in Select Examples?
While using ChemDraw Professional 21.0.0.28 to construct some cyclic allenes and rotationally restricted biphenyls, I came across anomalous assignments of stereochemistry. [For the latest version of ...
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Why this structure is diastereomers instead of enantiomers
In this diagram optical isomers has divided in to 2 categories, one is diastereomers and enantiomers. Is the example for diastereomers correct? For me its looks like enantiomers
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