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(a)
Interpretation:
Bond-line structure of aspartame and its three stereoisomers need to be drawn.
Concept introduction:
Bond-line structure is the representation of organic structural formulas in a shorthand manner. In this case only the bond between carbon and other atoms are shown except hydrogen. It is understood that all the remaining valency to be filled by hydrogen. Apart from carbon atoms the other atoms are shown along with hydrogen. For drawing a peptide sequence in bond-line structure the steps need to be followed are,
- Draw the peptide with correct number of residues
- The side chain associated with the residue has to be identified
- Assign proper configuration for the residues
To draw: bond-line structure of aspartame
(b)
Interpretation:
Bond-line structure of aspartame and its three stereoisomers need to be drawn.
Concept introduction:
Stereoisomers are the compounds which have the same structural entry but differ in the configuration at the chiral centers. If a compound has only one stereo center then that compound has one stereoisomer. If it has two stereocenters then that compound has four stereoisomers. The number of stereoisomers possible can be found out by a formula,
To draw: all the three stereoisomers of aspartame
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Chapter 25 Solutions
ORGANIC CHEMISTRY-STD.WILEY PLUS CARD
- Check all molecules that are acids on the list below. H2CO3 HC2H3O2 C6H5NH2 HNO3 NH3arrow_forwardFrom the given compound, choose the proton that best fits each given description. a CH2 CH 2 Cl b с CH2 F Most shielded: (Choose one) Least shielded: (Choose one) Highest chemical shift: (Choose one) Lowest chemical shift: (Choose one) ×arrow_forwardConsider this molecule: How many H atoms are in this molecule? How many different signals could be found in its 1H NMR spectrum? Note: A multiplet is considered one signal.arrow_forward
- For each of the given mass spectrum data, identify whether the compound contains chlorine, bromine, or neither. Compound m/z of M* peak m/z of M + 2 peak ratio of M+ : M + 2 peak Which element is present? A 122 no M + 2 peak not applicable (Choose one) B 78 80 3:1 (Choose one) C 227 229 1:1 (Choose one)arrow_forwardShow transformation from reactant to product, step by step. *see imagearrow_forwardCheck the box if the molecule contains the listed item. *See imagearrow_forward
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- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY
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