chiral. If you were able to make another molecule that is a mirror image of the chiral molecule,the mirror image and the original molecule will be non-superimposable. i.e. the atomssurrounding carbon won't completely align. The lack of alignment of the suround atom makesthe two molecules different from each other.The central carbon must be surrounded by 4 different groups. The chiral carbon is highlighted.CH;CH)CHICH2CH3-C-CH2-CHyOHCH)mirorThe 3D structure of the above molecule focuses on the chiral carbon and the bond surrounding thechiral carbon. The molecule on the left is different from the molecule on the right (mirror image)because they are non-superimposable.H.CH3-C-COOHHOOCCOOHCHNH2NH2mimorAnswer the following questions:1. Draw five structural isomers for hexane, CHe.Isomer 3Isomer 2Isomer 1Isomer 5Isomer 42. Draw three structural isomers as possible for CHO.

Answered: Image /qna-images/answer/d7f96766-95ab-439a-935b-1c5e6686f06c.jpg

chiral. If you were able to make another molecule that is a mirror image of the chiral molecule, the mirror image and the original molecule will be non-superimposable. Le. the atoms surrounding carbon won't completely align. The lack of alignment of the surround atom makes the two molecules different from each other. The central carbon must be surrounded by 4 different groups. The chiral carbon is highlighted. CH;CH) CHCH2 CH3-C-CH2-CHy OH CH3 mimor The 3D structure of the above molecule focuses on the chiral carbon and the bond surrounding the chiral carbon. The molecule on the left is different from the molecule on the right (mirror image) because they are non-superimposable. H. CH3-C-COOH HOOC CHI NH2 mimor Answer the following questions: 1. Draw five structural isomers for hexane, CHe Isomer 3 Isomer 2 Isomer 1 Isomer 5 Isomer 4

chiral. If you were able to make another molecule that is a mirror image of the chiral molecule, the mirror image and the original molecule will be non-superimposable. Le. the atoms surrounding carbon won't completely align. The lack of alignment of the surround atom makes the two molecules different from each other. The central carbon must be surrounded by 4 different groups. The chiral carbon is highlighted. CH;CH) CHCH2 CH3-C-CH2-CHy OH CH3 mimor The 3D structure of the above molecule focuses on the chiral carbon and the bond surrounding the chiral carbon. The molecule on the left is different from the molecule on the right (mirror image) because they are non-superimposable. H. CH3-C-COOH HOOC CHI NH2 mimor Answer the following questions: 1. Draw five structural isomers for hexane, CHe Isomer 3 Isomer 2 Isomer 1 Isomer 5 Isomer 4

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter12: Chirality

Section: Chapter Questions

Problem 16E

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Similar questions

Compounds that have non-superimposable mirror images are (select all possible answers) chiral. optically active. enantiomers. meso. identical. achiral.
Molecules without a plane of symmetry are chiral. In the model you constructed in no.1, the tetrahedral carbon is the stereocenter; the molecule is chiral. A simple test for a stereocenter in a molecule is to look for a stereocenter with four different atoms or groups attached to it; this molecule will have no plane of symmetry. label the stereocenter in each structure with an asterisk (*).
Chiral Molecules are those which have four different substituents attached to a central atom. They producee mirror image material that are superimpossable. Which of the statements is true? O None of the statement is true O Both statements are true O Only the second statement is true O Only the first statement is true
H ÇI CH3-C-COOH он CH3-C-CH2Br 1. ČI a b 81. Consider the structures above. Which of these two contains a stereocenter? Draw thestructure on your answer sheet and mark the stereocenter with an asterisk. 82. Which of these two is a chiral molecule? Explain your answer. 83. Which of these two can exist as a pair of enantiomers? 84. Draw the pair of enantiomers using three-dimensional representation.
.. O 2. Give the molecula formula for the following compounds and star the chiral center(s) in each one of them if there is any. HO NO2 HS N' HOOJ HN Но H. CH3 followingnotegu F. HOO) HO, CH3 HOO). N. ఆరింది 3. Define chiral and an achiral molecules. 4. Define structural (or constitutional isomers). Draw as many constitutional isomers as possible with a molecular formula of C6H14 5. Define stereoisomers and give an example of two stereoisomers (draw them in line-angle notation). 6. Define diastereomers and give an example of two diastereomers (draw them in line-angle notation). 7. Define enantiomers and give an example of two enantiomers (draw them in line-angle notation).
Are there any chiral centers present in these compounds? OH HO ..|| Br F Br NO2 CH3 H3C NO2
Determine the chiral center's configuration(s) [back to front].
How many chiral centers does this molecule have?
!
Determine the chiral centres.
4357). ve? 8. Assign the correct chiral center. A) S B) R C) cis D) trans E) meso NH₂
2. Draw the diastereomers for each of the molecules below. Indicate which ones are enantiomeric pairs. Hint: Use 2" where n= the number of chiral carbons.