Skip to main content

Questions tagged [stereochemistry]

Applicable to questions about the spatial arrangement of atoms in a molecule and how they affect its physical or chemical properties.

-1 votes
1 answer
48 views

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 ...
Leon Raj's user avatar
2 votes
1 answer
136 views

Point group of trimethyl borate $\ce{B(OCH_3)3}$

What's the point group of trimethyl borate $\ce{B(OCH_3)3}$. The answer that my teacher gave is $D_{3h}$ but I'm struggling to see the n perpendicular $C_2$ axes and the horizontal plane of reflection....
Joe's user avatar
  • 21
1 vote
1 answer
65 views

Stereochemical relationship of molecules including double bond configuration and absolute configuration

Are (S,E)-4-isopropoxypent-3-en-2-ol and (R,Z)-4-isopropoxypent-3-en-2-ol both enantiomers and diastereomers? I am a bit confused because they would be diastereomers when only looking at the ...
crvenikupus's user avatar
3 votes
0 answers
41 views

Systematic method to determine D/L notation of substances other than amino acids and glyceraldehyde

The fundamental rules of D/L notation, as I understand it, are as follows; In D/L notation, a molecule is named by mapping it to glyceraldehyde. The D/L notation is based on the stereo configuration ...
Blue Various's user avatar
3 votes
1 answer
156 views

If the substituents are distinguishable, is it possible to prioritize them using the CIP rules?

In the R/S stereochemical nomenclature, when we try to determine the priority of substituents around a chiral carbon, are there specific examples where the ranking cannot be definie under the CIP ...
Blue Various's user avatar
2 votes
2 answers
410 views

Does a chiral allene have stereogenic centres?

This a picture of what my professor taught in class. According the the definition of a stereogenic centre, allene should have two of them. So I don't understand what I am interpreting wrong.
Shikhar's user avatar
  • 39
0 votes
4 answers
337 views

Do conformations arise from vibrations?

I was wondering how a molecule transforms from one conformation to another. Surely, since the conformations are separated by a potential barrier, some activation energy must be required. The energies ...
ananta's user avatar
  • 2,304
2 votes
1 answer
99 views

How to determine the value of the NOE from the NOESY spectrum?

I have 1D NOESY spectra from which I need to find out the value of the NOE (%). Is it enough to simply measure the intensity of the resulting peaks or is it necessary to subtract it from the ...
Klee's user avatar
  • 21
0 votes
0 answers
202 views

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 > $C_3$ > $C_1$ &...
Naitik Mundra's user avatar
2 votes
1 answer
170 views

Explain the mechanism of the following reaction, which involves a 1,2-alkyl migration with double inversion of configuration

I came across the following reaction, whose mechanism is said to involve a 1,2-alkyl migration with a double inversion in configuration. The reagents used were nitrous acid (generated in situ) ...
Cyclopropanol's user avatar
0 votes
0 answers
46 views

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 ...
HasturQ's user avatar
  • 49
1 vote
1 answer
70 views

Fischer Projection for Different Compounds

Which of the following Fischer projections is different from the other? Just by looking at the R-S configuration, figure C is the odd one out. But when I look at D I see that both methyl and hydrogen ...
Anonymousstriker38596's user avatar
3 votes
1 answer
608 views

Are conformational isomers diasteromers?

I am currently struggling on seeing where exactly conformational isomers fit within stereochemistry & how (and whether) they are a subset of diasteromers. I've seen potentially conflicting ...
Mosrod's user avatar
  • 41
-1 votes
1 answer
28 views

9,10-dihydro-9,10-ethanoanthracene derivatives. Stereoisomers or different compounds? What are their chemical names?

What is the relationship between these compounds? Are they stereoisomers or some of them are different compounds? Additionally, what would be their names? (For position 9, with the methyl substituent) ...
Levis_olympus's user avatar
-3 votes
1 answer
331 views

How many aldehydes and ketones can be formed from molecular formula C5H10O? [closed]

Question: What are the possible aldehydes and ketones with molecular formula $\ce{C5H10O$ (including the stereoisomers)? Answer: 5 aldehydes and 3 ketones The degree of unsaturation of the compound ...
Prithuj Sarkar's user avatar

15 30 50 per page
1
2
3 4 5
56