Concept explainers
(a)
Interpretation:
Conjugated organic molecules has to be ranked based on decreasing
Concept introduction:
Conjugation on
HOMO-LUMO: In a
Auxochrome: When the molecule attached to a chromophores group the both
(b)
Interpretation:
Conjugated organic molecules has to be ranked based on decreasing
Concept introduction:
UV/vis spectroscopy: It is deal with information about various compounds that have conjugated double, the UV light and visible light have jest the right energy to cause an electronic transition in a molecule that is to promote an electron from one molecular orbital to another higher energy.
Conjugation on
HOMO-LUMO: In a
Auxochrome: When the molecule attached to a chromophores group the both
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EBK ORGANIC CHEMISTRY
- Muscalure is the sex attractant of the common housefly. Flies are lured to traps filled with bait that contain muscalure and an insecticide. Eating the bait is fatal. How could you synthesize muscalure using 1-bromopentane as one of the starting materials?arrow_forwardAs shown below, when compound 6a is heated, (1Z, 3Z)cycloheptadiene is formed. When the related compound 6b is heated, however, (1E, 3Z)-cyclodecadiene is formed. Explain these results, and suggest a reason why opening of the five-membered ring in 6a needs a higher temperature than that of the eight-membered ring in 6b. (7 points) H 270 °C H 6a 6b H 190 °Carrow_forwardORGANIC CHEMISTRY Justify the stereoselectivity of the following Diel Alders intramolecular reaction:arrow_forward
- (2R,3S)-2-Bromo-3-phenylbutane undergoes an E2 elimination when treated with sodium methoxide. Draw all possible Newman projections for the bond relevant for the elimination reaction, and use those Newman projections to explain the stereochemical outcome of the reaction. Draw the final product and provide its IUPAC name.arrow_forward(c) Rank the compounds in each group in order of decreasing ^ max : (i) -СН—СH- -CH=CH2 CH3 (i) CH3 H3C- CH3arrow_forwardHow many rings and π(pi) bonds are contained in compound A and draw one possible structure for this compound A. Compound A has molecular formula C6H10 and is hydrogenated to a compound having molecular formula C6H12arrow_forward
- Compound O has molecular formula C10H12O and shows an IR absorption at 1687 cm−1. The 1H NMR spectrum of O is given below. What is the structure of O?arrow_forwardCompound W O₂, H₂O₂ A Compound W could likely be: H3 CH₂ CH3 O B MgBr {₁ C MgBr Compound X Darrow_forwardAn unknown compound X has the molecular formula C10H1102 Br. Compound X shows a strong absorption in its IR spectrum at 1700 cm³1. The 1H NMR spectral data for compound X is given below. What is the structure of compound X? absorption doublet singlet 8 ratio 1.0 5.5 3 2 4.4 1 5 quartet broad singlet 7.2 Br Multiple Choice Only III I or II Only I Only II || Br III Brarrow_forward
- A key step in the synthesis of the narcotic analgesic meperidine (trade name Demerol) is the conversion of phenylacetonitrile to X. (a) What is the structure of X? (b) What reactions convert X to meperidine?arrow_forwardQ7arrow_forwardCompounds Y and Z are isomers with the molecular formula C10H12O. The IR spectrum of each compound shows a strong absorption band near 1710 cm−1 . The 1H NMR spectra of Y and Z are given below. Propose structures for Y and Z.arrow_forward