Achiral
Explanation :
because it is symmetric in such a way that it can be superimposed on its mirror image.
The molecule below is: OH o OH Optically active Non superimposible on its mirror image Both...
The molecule below is: ОН ОН Optically active Non superimposible on its mirror image Both (-) and (+) Achiral
QUESTION 14 Is the molecule shown below chiral or achiral? Explain what this means. CI CEO -C HyCH C O The molecule is chiral because its mirror image is nonsuperimposable. O The molecule is achiral because its mirror image is superimposable.
1) Label each of the following molecule as optically active (OA) or optically inactive (OD? (Type in your answer as OA or OL in the blank space below each structure) [6] OH 1:1 Mixture
Geometric Geometric Geometric 23. Organic molecules which are optically active and they are mirror images to each other are called....... Enantiomers. a. Chain isomers. d. Geometrical isomers c. Diastereoisomers. 24. The organic molecule that rotates the plane-polarized light to left is called a. Dextrorotatory b. Functional isomers c. Positional isomers d. levorotatory 25. The organic molecule that rotates the plane-polarized light to right is called a. Dextrorotatory b. Functional isomers c. Positional isomers d. levorotatory 26. Chiral molecules are organic...
Please help me!! 2. (4) True or False - Any molecule that does not have a plane of symmetry must be optically active _ The mirror image of a meso compound is its enantiomer and is chiral. El reactions go faster when run in water than in acetone. Rearrangements are often a complication in E2 reactions.
15 Enantiomers are? stereoisomers having non-identical mirror image configurations stereoisomers that do not have non-identical mirror image configurations stereoisomers having u mirror plane of symmetry achiral stereoisomers Which of the following structures represents a chiral compound? The correct IUPAC name for the following compound is:
2. What is a necessary condition for the occurrence of isomers that are optically active? 4. Which structural isomer of n-butyl alcohol, CH3CH2CH2CH,OH, could have a chiral center? 1. Which of the molecules shown can exhibit optical isomerism? Use an arrow to indicate the chiral center in each optically active molecule. 3. The structural formula of ibuprofen, an over-the- counter analgesic, is shown below. Use an arrow to in- dicate any chiral center. 4. One optical isomer of ibuprofen is...
please answer all Question 1 2 pts Determine whether the molecule below is optically active. cannot determine O optically active O optically inactive Question 2 2 pts Determine the relationship between the two molecules below NH2 HO H3COOH identical enantiomers constitutional isomers diastereomers Question 3 2 pts Determine the relationship between the two molecules below H HOW enantiomers O identical constitutional isomers diastereomers D Question 4 2 pts Determine the total number of stereoisomers represented by the bond line drawing...
7. (9 pts) (Are the following optically active or meso? meso HyCHC OH HO opticaly actve active opti call active 8. (3 pts) How many stereoisomers are there of 2,3-dibromobutane? 4 sleeoisamvers (8 pts) Circle the letter of the statements that are true. a. Racemic mixtures are optically active Enantiomers have specific rotations that are equal, but have opposite signs 9. o adtc) Achiral molecules are optically inactive d Meso compounds contain equal amounts of enantiomers 4pts) Complete the Fischer...
a chiral molecule id defined as one that is .... on its mirror image.