Concept explainers
(a)
Interpretation:
The expected products when the triglyceride containing one equivalent of stearic acid and two equivalents of oleic acid react with the given reagents is to be drawn and the products will be optical active or not is to be stated.
Concept introduction:
Chiral molecules are those molecules that consist of different groups or atoms around the centre atom. They don’t possess symmetry. Optical activity of compounds relies upon chirality. Only those compounds can rotate light that possess chiral centers.
(b)
Interpretation:
The expected product when the triglyceride containing one equivalent of stearic acid and two equivalents of oleic acid react with the given reagents is to be drawn and the product will be optical active or not is to be stated.
Concept introduction:
Chiral molecules are those molecules that consist of different groups or atoms around the centre atom. They don’t possess symmetry. Optical activity of compounds relies upon chirality. Only those compounds can rotate light that possess chiral centers.
(c)
Interpretation:
The expected product when the triglyceride containing one equivalent of stearic acid and two equivalents of oleic acid react with the given reagents is to be drawn and the product will be optical active or not is to be stated.
Concept introduction:
Chiral molecules are those molecules that consist of different groups or atoms around the centre atom. They don’t possess symmetry. Optical activity of compounds relies upon chirality. Only those compounds can rotate light that possess chiral centers.
(d)
Interpretation:
The expected products when the triglyceride containing one equivalent of stearic acid and two equivalents of oleic acid react with the given reagents is to be drawn and the products will be optical active or not is to be stated.
Concept introduction:
Chiral molecules are those molecules that consist of different groups or atoms around the centre atom. They don’t possess symmetry. Optical activity of compounds relies upon chirality. Only those compounds can rotate light that possess chiral centers.
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Chapter 25 Solutions
EP ORGANIC CHEMISTRY -MOD.MASTERING 18W
- Q1. (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_forwardWhich is NOT the typical size of a bacteria? 1000 nm 0.001 mm 0.01 mm 1 umarrow_forwardNonearrow_forward
- Show work. don't give Ai generated solutionarrow_forwardPart 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_forward
- SH 0 iq noitzouDarrow_forwardNonearrow_forward+ HCl →? Draw the molecule on the canvas by choosing buttons from the Tools (for bonas), Atoms and Advanced Template toolbars. The single bond is active by default. + M C + H± 2D EXP. CONT. K ? L 1 H₁₂C [1] A HCN O S CH3 CH 3 CI Br HC H₂ CH CH CH3 - P Farrow_forward
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