Chapter 24: Problem 94
Can a DNA strand bind to a complementary RNA strand? Explain.
Chapter 24: Problem 94
Can a DNA strand bind to a complementary RNA strand? Explain.
All the tools & learning materials you need for study success - in one app.
Get started for freeWhich statement best explains the chemical differences between DNA and RNA? (a) DNA has two different sugars in its sugar-phosphate backbone, but RNA only has one. (b) Thymine is one of the DNA bases, whereas RNA's corresponding base is thymine minus a methyl group. (c) The RNA sugar-phosphate backbone contains fewer oxygen atoms than DNA's backbone. (d) DNA forms double helices but RNA cannot.
(a) One test for the presence of an alkene is to add a small amount of bromine, which is a red-brown liquid, and look for the disappearance of the red-brown color. This test does not work for detecting the presence of an aromatic hydrocarbon. Explain. (b) Write a series of reactions leading to para-bromoethylbenzene, beginning with benzene and using other reagents as needed. What isomeric side products might also be formed?
Write the condensed structural formulas for two alkenes and one alkyne that all have the molecular formula \(\mathrm{C}_{6} \mathrm{H}_{10}\) .
A typical amino acid with one amino group and one carboxylic acid group, such as serine, can exist in water in several ionic forms. (a) Suggest the forms of the amino acid at low pH and at high pH. (b) Amino acids generally have two pK\(_{a}\) values, one in the range of 2 to 3 and the other in the range of 9 to \(10 .\) Serine, for example, has pK\(_{a}\) values of 2.19 and \(9.21 .\) Using species such as acetic acid and ammonia as models, suggest the origin of the two pK\(_{a}\) values. (c) Glutamic acid is an amino acid that has three \(\mathrm{p} K_{a}^{\prime} \mathrm{s} : 2.10,4.07,\) and \(9.47 .\) Draw the structure of glutamic acid, and assign each \(\mathrm{pK}_{a}\) to the appropriate part of the molecule. (d) An unknown amino acid is titrated with strong base, producing the following titration curve. Which amino acids are likely candidates for the unknown?
(a) When cyclopropane is treated with HI, 1 -i-iodopropane is formed. A similar type of reaction does not occur with cyclopentane or cyclohexane. Suggest an explanation for cyclopropane's reactivity. (b) Suggest a method of preparing ethylbenzene, starting with benzene and ethylene as the only organic reagents.
What do you think about this solution?
We value your feedback to improve our textbook solutions.