Lets have fun .never ask the hell like question.
Suspension.
I do not know tell me
your eyesight
the correct answer would be -( magnetic attraction of one part )
11.25 mg
its called a racemic mixture and is optically inactive
A racemic mixture with equal amounts of both enantiomers. Since achiral starting materials do not have any inherent chirality, their reaction products will not have a preference for forming one enantiomer over the other, resulting in a racemic mixture.
A racemic mixture is a combination of equal amounts of two enantiomers, which are molecules that are mirror images of each other but cannot be superimposed. This results in a mixture that is optically inactive, as the optical activities of the two enantiomers cancel each other out. Racemic mixtures are common in pharmaceuticals, where one enantiomer may have the desired therapeutic effect while the other may be inactive or even harmful. The process of separating enantiomers from a racemic mixture is known as resolution.
The SN1 mechanism is significant in the formation of a racemic mixture because it involves the formation of a carbocation intermediate, which can react with both enantiomers of a chiral nucleophile, leading to the production of equal amounts of both enantiomers in the final product. This results in a racemic mixture, where both the R and S enantiomers are present in equal amounts.
In an SN1 reaction, a racemic mixture is formed due to the random attack of the nucleophile on the carbocation intermediate, resulting in the formation of both R and S enantiomers in equal amounts.
racemization is defined as if we add cis and anti form it give rise to racemic mixture
In chemistry, a racemic mixture is one that has equal amounts of left- and right-handed enantiomers of a chiral molecule. The first known racemic mixture, or racemate, was 'racemic acid', which Pasteur found to be a mixture of the two enantiomeric isomers of tartaric acid. A racemate is optically inactive: because the two isomers rotate plane-polarized light in opposite directions they cancel out, therefore a racemic mixture does not rotate plane-polarized light. In contrast to the two separate enantiomers, which generally have identical physical properties, a racemate often has different properties compared to either one of the pure enantiomers. Different melting points and solubilities are very common, but different boiling points are also possible.
Enantiomers can have very different effects on the body, which contains many chiral compounds. While one enantiomer may have a healing medicinal effect, the other can be harmful, or at best, ineffective. While it is much more complicated to make a single enantiomer or separate a racemic mixture, taking a single-enantiomer drug often has a much greater effect.
A racemic mixture of lactic acid, which contains equal amounts of both enantiomers (D- and L-lactic acid), can be resolved using methods like selective crystallization, where one enantiomer is preferentially crystallized out of the mixture. Another common method involves enzymatic resolution, where specific enzymes selectively react with one enantiomer, allowing the other to remain unreacted. Additionally, chiral chromatography can be employed to separate the enantiomers based on their interaction with a chiral stationary phase. These techniques help isolate the desired enantiomer for further use.
Racemic mixture of tartaric acid consists of equal amounts of its D- and L-enantiomers, resulting in a 1:1 ratio. This forms a structure that lacks optical activity because the optical rotations of the enantiomers cancel each other out.
You depend on the physical state of the constituents to separate a mixture
separate a mixture