Chirality is the fundamental behind the optical activity of an organic molecule.
Chiral center: A‘C’ atom in a molecule becomes a chiral center when all the four valences of that atom are satisfied by chemically different groups. For a carbon to act as chiral center, it should be hybridization
The absence of symmetry is known as asymmetry. The carbon atom bonded to four unlike groups is called the asymmetric carbon which is also known as the chiral carbon.
In a non-chiral compound, the plane of symmetry is present and it does not have a chiral center.
The plane of symmetry: The plane of the mirror that cuts the compound into two equal halves.
Representative example for chiral center and optical isomers is given below:
Here C is bonded to four different groups A, B C and D, Thus, it forms two optical isomers as the mirror images of each other
(1)
Assume the given structures as follows:
Structure 1:
Structure 2:
Structure 3:
There is no asymmetric carbon in methylcyclohexane.
(2)
If a molecule is not chiral, then it has a plane of symmetry.
Structure 1:
Structure 2:
Structure 3:
Ans: Part 1
The asymmetric carbons in the given structures are indicated as follows:
Part 2
The plane of symmetry element is indicated for the given structures as follows:
Highlight, by clicking on, the asymmetric carbons (if any) in each structure. A selected atom will...
Highlight, by clicking on, the asymmetric carbons (if any) in each structure. A selected atom will turn green. Indicate whether each compound is chiral and the number of stereocenters (see Hint) in each molecule achiral chiral no stereocenters one stereocenter two stereocenters three stereocenters achiral chiral no stereocenters one stereocenter two stereocenters three stereocenters
Highlight, by clicking on, the asymmetric carbons (if any) in each structure. A selected atom l turn green. Cl CH2 CH3 H3C Indicate whether each compound is chiral and the number of stereocenters (see Hint) in each molecule. □ achiral □ chiral □ no stereocenters □ one stereocenter □ two stereocenters □ three stereocenters □ achiral □ chiral □ one stereocenter □ three stereocenters no stereocenters two stereocenters
Highlight - by clicking on - the chirality center(s), if any, in each structure. A selected atom will turn green. Click again to deselect your choice.
Select all of the asymmetric carbon atoms in the following structure. A selected atom will turn green. Select all of the asymmetric carbon atoms in the following structure. A selected atom will turn green.
5-26 For each structure, 1. star (*) any asymmetric carbon atoms. 2. label each asymmetric carbon as (R) or (S). draw any internal mirror planes of symmetry. label the structure as chiral or achiral. label any meso structures. We were unable to transcribe this image
How many asymmetric carbons are present in the compound below? Label each asymmetric carbon in the compound below as R or S. Draw this structure of (S)-1-bromo-1-chioropropane. Take particular care to indicate three-dimensional stereo chemical detail properly. Draw the Fischer projection of (S)-2-bromobutane.
please solve them clear & be sure thank you . 1. (21 points) Is the following compound a meso-compound? If yes, show it in 3D in the box below using wedged and dashed bonds to indicate the substituent bond direction and draw the internal mirror plane of symmetry (if any). (3 points) HOOC-CHOH-CHOH-COOH Draw the 3D structures of the stereoisomers of the compound above. Use wedged and dashed bonds to indicate the substituent bond direction in each stereoisomer. [Hint: if...
1. For each of the structure star asymmetric carbon atoms, Lab with R and Sand draw any internal mirror plane of symmetry and label chiral or achiral molecules and meso structures H3C CH2Br OH I Br H -ОН HOH CI Н. TH Br H Br H OH HH CH2Br CH2CH3 a b C Br Br CI CI d СН3 CH3 CH3 ...Н H ОН CHз CHз нас CH3 f е
15) How many asymmetric carbons are present in the compound below? нонс Ho OH OH 16) How many asymmetric carbons are present in the compound below? ÇOH но- H OH H OH COZH 17) How many asymmetric carbons are present in the compound below? -ethyl-2,2,4-trimethylpentane 18) Can the molecule shown below be properly described as a meso compound? B 19) Can the molecule shown below be properly described as a meso compound? 20) Can the molecule shown below be properly...
Identify the allylic carbons in each of the following structures. (Click on an atom to select it. Selected atoms will turn green. If you make a mistake, click on the atom again to deselect it.)