Determine if the following linear chain molecules are enantiomers, diastereomers, meso, the same molecule or constitutional isomers. When identifying the type of isomerism, compare pair by pair. JUSTIFY your answer. Use R/S to check for stereoisomerism, name each structure to check for constitutional isomerism. A D بالديدان B E F

Determine if the following linear chain molecules are enantiomers, diastereomers, meso, the same molecule or constitutional isomers. When identifying the type of isomerism, compare pair by pair. JUSTIFY your answer. Use R/S to check for stereoisomerism, name each structure to check for constitutional isomerism. A D بالديدان B E F

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter12: Chirality

Section: Chapter Questions

Problem 6E

See similar textbooks

Similar questions

Write the concept of a molecule that is classified as a meso form. Write an example that shows the difference between an enantiomer, a diastereomer, a meso form.
If the asymmetric carbons in a molecule have been designated (2R,3S,5R), what will the designations be in the molecule’s enantiomer? What will the designations be in one of its diastereomers?
Refer to the following molecule: CH,CH, Br H. H,C NO2 How many achiral carbons are there? Select ] The molecule is chiral. [ Select] What is the configuration on C2? [Select ] Does the molecule have a meso isomer? [ Select ] How many stereoisomers does the molecule have (including the one already shown)? [ Select ] How many diastereomer pairs does the molecule have? [Select] If the -NO2 and -Br switched places, the new compound will be [Select] with the original compound. What is the third priority substituent on carbon 2? Select]
Are these two molecules... functional isomers? Positional isoners? Enantiomers? Diastereomers? Meso isomers?
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.
How many asymmetric/chiral centers are present in the molecule below?
3. Draw the structural formula of 3-bromo-2-chloropentane. Identify the chiral carbons with asterisks. Using 2n formula (n is number of chiral centers) calculate the number of stereoisomers. Construct 2 pairs of mirror images. Take one pair of the enantiomers, compare it with the either of the models of the second pair of enantiomers. Are these two molecules mirror images? Draw the fisher projections of the four stereoisomers and identify diastereomers.
Are these molecules.... conformers? Enantiomers? Diastereomers? Meso compounds?
NH2 CH3
Compounds that have non-superimposable mirror images are (select all possible answers) chiral. optically active. enantiomers. meso. identical. achiral.
Use models (or drawings) to determine which of the following compounds are stable chiral molecules at room temperature. For those that are chiral, draw three-dimensional ( perspective) diagrams of the enantiomeric forms.
Glycosaminoglycans (GAGs) are heteropolysaccharides composed of repeating disaccharide units. These units have some similar characteristics that allow them to be identified as GAGS. Which of the structures are examples of glycosaminoglycans? А. C. E. HO HO COO™ H Н ОН Н CH₂OH H H H OH OH Н CH₂OH Н OH H ОН o,so H H Н CH₂OH H H ОН H CH₂OSO H NH C=0 CH, H H Н NH c=0 CH3 H CH,OH OH Н ОН OH H B. D. Н НО H ОН H CH₂OH H ОН Н СОО ОН Н Н H H OSoz H Н OH б H CH₂OH ОН CH₂OSO H ОН H Н OSO, H Н NHSO,