For mesotartaric acid, the correct configuration for chiral carbon is:

2 R, 3 S

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2 R, 3 R

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2 S, 3 R

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1 D, 2 L

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Solution

The correct option is C $2 S, 3 R$
First priority will be given to $O H$ and then to $C O O H$ .

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Similar questions

It is given that when (±)-2,3-dibromobutane reacts with $K O H$ , some of the products formed are:

Explain via mechanism and then choose the correct ones from the following.

Monosubstitution of (2S,3S)-2,3-dibromobutane using $O H^{-}$ yields a mixture of products.
Monosubstitution of (2S,3S)-2,3-dibromobutane using $O H^{-}$ yields a single major product.
Monosubstitution of (2R,3R)-2,3-dibromobutane using $O H^{-}$ yields a mixture of products.
Monosubstitution of (2S,3S)-2,3-dibromobutane using $O H^{-}$ yields a mixture of products.

Q. If

2 n \sum r = 0 a_{r} (x - 2)^{r} = 2 n \sum r = 0 b_{r} (x - 3)^{r}

and

a_{k} = 1

for all

k \geq n,

then

b_{n}

is equal to

Q. Subtract the following :

3 r + 2 t

from

2 r - 3 t

Q. Add:

6 p + 4 q - r + 2 r - 5 p - 6, 11 q - 7 p + 2 r - 1

and

2 q - 3 r + 4

You take two resistors of resistance 2 R and 3R and connect them in parallel in an electric circuit. Calculate the ratio of electric power consumed by 2 R and 3R.

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For mesotartaric acid, the correct configuration for chiral carbon is:

The correct option is C 2S,3RFirst priority will be given to OH and then to COOH.

The correct option is C $2 S, 3 R$
First priority will be given to $O H$ and then to $C O O H$ .