Concept explainers
Interpretation:
The optical activity for the given compounds is to be deduced and open-chain structure for the aldaric acid is to be written. Fischer projection formulas for D-threose and its nitric acid oxidation product is to be written and name of aldaric acids produced from D-erythrose and D-threose is to be deduced.
The structural formulas of the given compounds are to be represented and the true or false nature of the statements based on the optical activity for the given compounds, is to be deduced.
Concept introduction:
舧 A carbohydrate is a
舧
舧 Carbohydrates are oxidized by
舧 Aldaric acids are carbohydrates having two
舧
The molecules that are nonsuperimposable or not identical with their mirror images are known as chiral molecules.
舧 A pair of two mirror images that are nonidentical is known as enantiomers, which are optically active.
舧 The stereoisomers that are nonsuperimposable on each other and not mirror images of each other are known as diastereomers.
舧 The achiral compounds in which plane of symmetry is present internally and consists of chiral centres are known as meso compounds, but they are optically inactive.
舧 Compounds that have a plane of symmetry tend to exist in meso forms. A meso form arises when the two stereoisomers produce superimposable images, and hence, compounds having meso forms are optically inactive.
舧 When the order of progression from the group of highest priority to that of the next highest priority is clockwise, it is said to be the
舧 When the order of progression from the group of highest priority to that of the next highest priority is anticlockwise, then it is said to be the
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ORGANIC CHEM. VOL.1+2-W/WILEYPLUS
- Nonearrow_forwardDraw the structure of the product of the reaction given the IR and MS data. Spectral analysis of the product reveals: MS: M 150, M-15, M-43 CH.COCI AICI, IR: 3150-3000 cm, 2950-2850 cm and 1700 cmarrow_forwardPart II. Identify whether the two protons in blue are homotopic, enantiopic, diasteriotopic, or heterotopic. a) HO b) Bri H HH c) d) H H H Br 0arrow_forward
- Nonearrow_forwardChoose the option that is decreasing from biggest to smallest. Group of answer choices: 100 m, 10000 mm, 100 cm, 100000 um, 10000000 nm 10000000 nm, 100000 um, 100 cm, 10000 mm, 100 m 10000000 nm, 100000 um, 10000 mm, 100 cm, 100 m 100 m, 100 cm, 10000 mm, 100000 um, 10000000 nmarrow_forwardQ1. (a) Draw equations for homolytic and heterolytic cleavages of the N-H bond in NH3. Use curved arrows to show the electron movement. (b) Draw equations for homolytic and heterolytic cleavages of the N-H bond in NH4*. Use curved arrows to show the electron movement.arrow_forward
- Part II. count the expected number of signals in the 1H-NMR spectrum of these compounds HO 0 одев * Cl -cl "D"arrow_forwardPart I. Create a splitting tree diagram to predict the multiplet pattern of proton Hb in the compound below: 3 (Assume that "Jab >>> ³JbC) Ha Hb He он Ha NH2 Ha HCarrow_forwardNonearrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning