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A compound with the molecular formula C6H15N gave the following 1H NMR spectrum: triplet, 0 0.90
Quartet, 2.4
There were no other signals.The most likely structure for the compound is:
Diastereomers
Stereoisomers characterized by having distinct physical properties and not being mirror reflections of one another.
(2R,4R)-2,4-dibromopentane
A chiral compound with a specific configuration, indicating the presence of bromine atoms on the second and fourth carbon of a five-carbon chain.
Fischer Projection
A method of drawing organic molecules by projecting a three-dimensional molecule onto a two-dimensional plane.
Diastereomers
Stereoisomers that are not mirror images of each other, having two or more stereocenters and differing in the configuration at one or more of these centers.
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