Organic Chemistry
9th Edition
ISBN: 9781305080485
Author: John E. McMurry
Publisher: Cengage Learning
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Textbook Question
Chapter 1.SE, Problem 44AP
Quetiapine, marketed as Seroquel, is a heavily prescribed antipsychotic drug used in the treatment of schizophrenia and bipolar disorder. Convert the following representation into a skeletal structure, and give the molecular formula of quetiapine.
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Draw one possible structure for each of the following compounds based on the descriptions below.
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Chapter 1 Solutions
Organic Chemistry
Ch. 1.3 - Give the ground-state electron configuration for...Ch. 1.3 - How many electrons does each of the following...Ch. 1.4 - Prob. 3PCh. 1.4 - Convert the following representation of ethane,...Ch. 1.4 - What are likely formulas for the following...Ch. 1.4 - Prob. 6PCh. 1.4 - Prob. 7PCh. 1.7 - Draw a line-bond structure for propane, CH3CH2CH3....Ch. 1.7 - Convert the following molecular model of hexane, a...Ch. 1.8 - Draw a line-bond structure for propene, CH3CH=CH2....
Ch. 1.8 - Draw a line-bond structure for 1, 3-butadiene,...Ch. 1.8 - Following is a molecular model of aspirin...Ch. 1.9 - Draw a line-bond structure for propyne, CH3C≡CH....Ch. 1.10 - Prob. 14PCh. 1.12 - Prob. 15PCh. 1.12 - Prob. 16PCh. 1.12 - The following molecular model is a representation...Ch. 1.SE - Convert each of the following molecular models...Ch. 1.SE - The following model is a representation of citric...Ch. 1.SE - The following model is a representation of...Ch. 1.SE - The following model is a representation of...Ch. 1.SE - How many valence electrons does each of the...Ch. 1.SE - Give the ground-state electron configuration for...Ch. 1.SE - Prob. 24APCh. 1.SE - Prob. 25APCh. 1.SE - Draw an electron-dot structure for acetonitrile,...Ch. 1.SE - Draw a line-bond structure for vinyl chloride,...Ch. 1.SE - Fill in any nonbonding valence electrons that are...Ch. 1.SE - Convert the following line-bond structures into...Ch. 1.SE - Convert the following molecular formulas into...Ch. 1.SE - Prob. 31APCh. 1.SE - Oxaloacetic acid, an important intermediate in...Ch. 1.SE - Prob. 33APCh. 1.SE - Potassium methoxide, KOCH3, contains both covalent...Ch. 1.SE - What is the hybridization of each carbon atom in...Ch. 1.SE - Prob. 36APCh. 1.SE - Prob. 37APCh. 1.SE - What bond angles do you expect for each of the...Ch. 1.SE - Propose structures for molecules that meet the...Ch. 1.SE - What kind of hybridization do you expect for each...Ch. 1.SE - Pyridoxal phosphate, a close relative of vitamin...Ch. 1.SE - Prob. 42APCh. 1.SE - Prob. 43APCh. 1.SE - Quetiapine, marketed as Seroquel, is a heavily...Ch. 1.SE - Tell the number of hydrogens bonded to each carbon...Ch. 1.SE - Why do you suppose no one has ever been able to...Ch. 1.SE - Allene, H2C=C=CH2, is somewhat unusual in that it...Ch. 1.SE - Allene (see Problem 1-47) is structurally related...Ch. 1.SE - Complete the electron-dot structure of caffeine,...Ch. 1.SE - Most stable organic species have tetravalent...Ch. 1.SE - A carbanion is a species that contains a...Ch. 1.SE - Divalent carbon species called carbenes are...Ch. 1.SE - There are two different substances with the...Ch. 1.SE - There are two different substances with the...Ch. 1.SE - There are two different substances with the...Ch. 1.SE - Prob. 56APCh. 1.SE - Among the most common over-the-counter drugs you...
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- Write the chemical formula, bond-line structure, and condensed formula of undecanoic acid, and draw its bond line structure.arrow_forwardDraw structures that fit each description and name the functional group in each molecule: (a) two constitutional isomers with molecular formula C5H10O that contain different functional groups; (b) two constitutional isomers with molecular formula C6H10O that contain the same functional group.arrow_forward||| O NAMING AND DRAWING ORGANIC MOLECULES Interpreting condensed chemical structures Use this condensed chemical structure to complete the table below. 0 NH₂ - CH — C — OH | CH3 The condensed chemical structure of alanine Some facts about the alanine molecule: number of carbon-carbon single (C - C) bonds: number of carbon-hydrogen single (C-H) bonds: number of oxygen-hydrogen single (O - H) bonds: number of nitrogen-hydrogen single (N - H) bonds: number of lone pairs: X Ś 0 ☐ 1 D 503 Jessarrow_forward
- In a laboratory experiment, one sherbet lemon sweet produced 6.00 mL of carbon dioxide. d) Calculate the minimum mass (g) of tartaric acid necessary to produce this 6.00 mL volume of carbon dioxide. (Assume that 1 mole of carbon dioxide occupies 24.0 L at room temperature and pressure). e) By making the appropriate substitutions for tartaric acid's H (hydrogen) and OH (hydroxyl) groups among positions A, B, D and E in the structure shown below, how many different stereoisomers of tartaric acid are possible? HO₂C B CO₂H A Earrow_forwardIdentify and label all functional groups of Carvone (alcohols, amines, amides, carboxylic acids, ketones, aldehydes, aromatic rings, aromatic amines, etc) on the Lewis Structure. You do not have to circle alkanes.arrow_forwardFor which compound containing a heteroatom (an atom other than carbon or hydrogen) does the molecular ion have an even-numbered mass? For which does it have an odd-numbered mass? Q.)A primary amine with the molecular formula CnH2n-1NH2arrow_forward
- Provide the IUPAC name for the following molecules. In your answer, include a description of how the name was derived. но Identify the hybridisation of all the carbon, oxygen and nitrogen atoms in the following molecules. OHarrow_forwardProteins are made of amino acids. Given below is the structure of an example of amino acid. What are the two functional groups found in all amino acids? H CH3 | T + H-N-C-C T H H O carboxylate group and methyl group O ammonium group and methyl group O methyl group and thiol group O aldehyde group and ketone group O ammonium group and carboxylate group Oarrow_forwardWrite the molecular formula for the following line structures: Oarrow_forward
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