What is the correct structure for D-glucopyranose? What is the relationship between the following compounds? a) anomers b) meso compounds c) enantiomers d) equivalent structures What is the relationship between the following compounds ? a) anomers b) meso compounds c) enantiomers d) equivalent structures
1) Use the synthetic division to find: f(-2) f(x)= 2x^2 - 3x^2 + 7x - 12 2) For the function f(x) = -x^3 + 8x^2 - 40 Show how to use synthetic division to find out if -1 is a zero. 3) One of the zeros of the function f(x) = x^3 - 7x^2 + 17x - 15 is 2-i. Find all the other zeros 4) Use the intermediate value theor
(See attached file for full problem descriptions) D. Assume you have a mixture of the three amino acids. Predict the electrophoresis pattern you would expect to see at pH 7.6. Explain your prediction by indicating charges expected on each amino acid at pH 7.6 3. The amino acid, isoleucine, is shown attached. Show what re
I need some help with these questions: A. Explain the following NMR spectrum for N,N - Dimethylformamide. At room temperature, three peaks are observed: 1. 2.9 (singlet, 3H) 2. 3.0 (singlet 3H) 2. 8.0 (singlet, 1H) As the temperature is raised, only 2 peaks are observed: 1. 2.95 (singlet, 6H) 2. 8.0 (singlet, 1H) B.
5. Show the products of the following reagents (see attached file) with p-methylbenzoic acid. 6. Match the compounds with the following boiling points. Be sure to explain your selections in terms of intermolecular forces involved (see attached file). (See attached file for full problem description)
A. Draw structures for the following compounds (see attached file) B. Name the following compounds (see attached file) C. Rank the following compounds in terms of increasing acidity. Explain your reasoning. (see attached file) (See attached file for full problem description)
1. Which of the isomeric amines below has a higher boiling point? Explain your reasonsing and make a drawing to illustrate the intermolecular forces involved: (CH3 -CH2-CH2)3-N vs. CH3-(CH2)8-NH2 2. Show the reagents needed to synthesize 1-propanamine from the following: CH3CH2CHO CH3CH2CN CH3CH2CONH2 3. Name t
1. What are the ingredients of a cephalin? 2. Which fatty acid is always unsaturated in a cephalin? Why? 3. What is the enzyme system used in the formation of the prostalandins and thromboxanes? 4. Would you expect sodium ions (Na+) to be able to pass easily into a cell through bi-layer membrane wall? Why or Why not?
Methanol, Ethanol, & 1-Propanol 1) How would you sketch these three alcohol molecules? 2) What is each of their polarity? 3) What differences might you expect in the comparative solubility of each of them in lipids? WHY??? 4) If you were to add 2 drops of sheep blood to each of these alcohols (about 1/3 of a small te
In the mass spectrum of butylbenzene, the base peak occurs at m/z a. 134 b. 119 c. 105 d. 91 The number of mono-bromination products of p-xylene is a. 1 b. 2 c. 3 d. 4 Which of the following compounds has the lowest boiling point? a. p-dichlorobenzene b. o-dichlorobenzene c. m-
I need some help with answering these questions: (See attached file for full problem description and structural formulas) 1. Predict whether the molecule would be expected to show aromatic character or not. Explain your answer. 2. What is the hybridization of the nitrogen atom in sulfathiazole? 3. Assuming that the sulfur
6. The mass spectrum and the infrared spectrum for an unknown hydrocarbon are shown below. From this information, suggest a structure for the hydrocarbon. Indicate on the spectra how your structure fits the data. (See attached file for full problem description)
4. Infrared Spectroscopy (a) Deduce a possible structure for the compound with the following major IR absorptions. Explain your choice based on the IR absorptions, indicating the absorptions on your molecule. C4H8O: 3000, 2850 (weak), 2715 (weak), 1730 (strong) cm^-1. (b) How could you use IR spectroscopy to distinguish betw
Absorption of UV-visible energy by a molecule results in: a. vibrational transitions b. rotational transitions c. proton flips d. electronic transitions. 2. Which of the following compounds absorbs the longest wavelength of UV-visible light? a. 2-butene b. 1,4-hexadiene c. 1,3-hexadiene
Benzene is a organic solvent with the formula, CB6BHB6B. It boils at 80.1 C and melts at 5.5 C. Benzene's density is 0.88 gm/ml, its heat of vaporization is 20.0 KJoules per mole, its heat of fusion is 10.0 KJoules per mole, its heat capacity is 0.50 KJoules per mole-degree C for liquid benzene, 0.25 KJoules per mole-degree C fo
Please see the attached for diagram. What is the number of carbon atom that determines whether the carbohydrate shown below belongs to the D series or to the L series? a. 1 b. 2 c. 3 d. 4 e. 5
Please see attached The fact that glucose undergoes mutarotation is best explained by a. righ flipping between nonequivalent chair conformations by the b-pyranose form. b. interconversion of the alpha and beta pyranose forms. c. interconversion of aldehyde and enol forms d. interconversion of aldehyde and ketone forms e.
Each of the following statements about fructose is correct except one. Which statement is incorrect? a. Fructose is a stereoisomer of glucose b. Fructose has six carbon atoms c. Fructose is a monosaccharide d. Fructose is a ketose
Each of the following statements about glucose is correct except one. Which statement is incorrect? a. Glucose is an aldose b. Glucose is a hexose c. There are 14 diastereomers of glucose (in its open-chain form). d. Glucose is a monosaccharide e. Glucose is a stereoisomer of ribose.
Show that you know how to make the compound shown int he attachment by identifying the first step in its synthesis from 1-bromobutane. With which of the following would you treat 1-bromobutane in the first step?
1. Unbalanced equation SOCL2(1) + H2O(1) --- SO2(g) + HCl(g). How many molecules of H2O can 35.0 grams of thionyl chloride remove? 2. An experiment that led to the formation of the new field of organic chemistry involved the synthesis of urea, CN2H40, by the controlled reaction of ammonia and carbon dioxide: gaseous ammonia +
89. A) We often hear the terms organic, natural, and chemical in the media. Organic and natural are usually used to imply that a product is "healthy" and/or "environmentally friendly" while chemical often implies negative implications for health and for the environment. In your opinion, are these implications justified? Us
Which one of the following compounds undergoes nitration of its aromatic ring(electrophillic aromatic substitution) at the fastest rate: Benzene, Chlorobenzene, Nitrobenzene, Anisole, or Ethylbenzene?
(See attached file for full problem description) The structure of biphenyl and the numbering scheme used in naming its derivatives are indicated below. What is the major product obtained on dinitration of biphenyl?
1. A solution of 0.5g (-)-epinephrine dissolved in 10mL of dilute HCl was placed in a 20-cm polarimeter tube. Its optical rotation in sodium line (light wavelenth) was -5.0 degrees at 25 degrees Celsius. What is the specific rotation of the (-)-epinephrine? 2. Calculate the enantiomeric excess (e.e.), a measure of optical p
1. The compound hexane, CH3-CH2-CH2-CH2-CH2-CH3 has how many tertiary hydrogens? 2. How many monobromination products of pentane might be expected?
2. Consider the molecule cyclohexane, which contains only hydrogen and carbon atoms. a) When a sample is burned in oxygen, 4.822 g of CO(2) and 1.650g of H(2)O are obtained. What is its simplest formula? b) Calculate the mass percent of carbon and hydrogen in cyclohexene. c) How many grams of carbon would you obtain fro
Explain why compound A reacts 9000 times faster than compound B at 0 degrees, but the two compounds react at the same rate at 103 degrees.
1. Which of the following molecules has NO net molecular dipole? a. CH3OH b. CH2O c. CH3Cl d. H2C=CH2 2. Which of the following molecules can hydrogen bond to another of the same compound? a. CH3CH2OCH2CH3 b. CH3CH2COOCH3 c. (CH3CH2)2CHOH d. CH3CH2COCH2CH3 3. What term best describes the relationship betwe
Which of the following hydrocarbons is reduced by sodium in liquid ammonia: 1-Pentene, 2-Pentyne, 1,3-Pentadiene, or 1,4-Pentadiene