Determine whether each structure is likely to be colored or not. For those that you predict to be colored, indicate the extended conjugation by marking the series of continuous sp2 hybridized atoms.
(a)
(b)
(c)
Determine whether each structure is likely to be colored or not. For those that you predict to be colored, indicate the extended conjugation by marking the series of continuous sp2 hybridized atoms.
(a)
(b)
(c)
Identify the following dienes as being in the s-cis or s-trans conformation. If they are in the s-trans conformation, draw them in the s-cis conformation. [It may not always be possible.]
(e)
A 4.0 × 10-5 M solution of a compound in hexane shows an absorbance of 0.40 at 252 nm in a cell with a 1 cm light path. What is the molar absorptivity of the compound in hexane at 252 nm?
Hexa-1,3,5-triene uses six p orbitals, each containing a single electron, to make its three π bonds. How many total molecular orbitals are made by the six p orbitals?
Determine whether each structure is likely to be colored or not. For those that you predict to be colored, indicate the extended conjugation by marking the series of continuous sp2 hybridized atoms.
(g)
Identify the following dienes as being in the s-cis or s-trans conformation. If they are in the s-trans conformation, draw them in the s-cis conformation. [It may not always be possible.]
(c)
For the following terpenes, identify the isoprene units. In cross-linked or ring-containing terpenes, linkages can be formed between more than just C1 and C4 of isoprene.
(a)
Identify the isoprene units in the terpenes shown. In cross-linked or ring-containing terpenes, linkages can be formed between more than just C1 and C4 of isoprene.
(a)
What would be the difference in the colors of the compounds at pH = 3?
Phenolphthalein is an acid–base indicator that is colorless below pH 8 and red above pH 8. Explain briefly why the first structure is colorless and the second structure is colored.
Which statement is true about bacterial conjugation?
Answer the following questions for the molecular orbitals (MOs) of 1,3,5,7-octatetraene:
g. How many nodes does the highest-energy MO of 1,3,5,7-octatetraene have between the nuclei?
One milligram of a compound of molecular weight 160 is dissolved in 10 mL of ethanol, and the solution is poured into a 1-cm UV cell. The UV spectrum is taken, and there is an absorption at λmax = 247 nm. The maximum absorbance at 247 nm is 0.50. Calculate the value of e for this absorption.
What is commonly shared between bacteria through the process of conjugation?