Organic Chemistry
9th Edition
ISBN: 9781305080485
Author: John E. McMurry
Publisher: Cengage Learning
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Textbook Question
Chapter 1.SE, Problem 29AP
Convert the following line-bond structures into molecular formulas:
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Following is a structural formula of the prescription drug famotidine, marketed by McNeil Consumer Pharmaceuticals Co. under the name Pepcid. The primary clinical use of Pepcid is for the treatment of active duodenal ulcers and benign gastric ulcers. Pepcid is a competitive inhibitor of histamine H2 receptors that reduces both gastric acid concentration and the volume of gastric secretions.
Q. Complete the Lewis structure of famotidine showing all valence electrons and any formal positive or negative charges.
Give the Expanded Lewis Structure and Bond Line Structure of the given compound. (kindly refer to the image below)
Drawing resonance structures shows ways a molecule vibrates back and forth between two differnt bond-line structures.
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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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- Vitamin B6 is an organic compound whose deficiency in the human body can cause apathy, irritability, and an increased susceptibility to infections. Below is an incomplete Lewis structure for vitamin B6. Complete the Lewis structure and answer the following questions. Hint: Vitamin B6 can be classified as an organic compound (a compound based on carbon atoms). The majority of Lewis structures for simple organic compounds have all atoms with a formal charge of zero. Therefore, add lone pairs and multiple bonds to the structure below to give each atom a formal charge of zero. a. How many bonds and bonds exist in vitamin B6? b. Give approximate values for the bond angles marked a through g in the structure. c. How many carbon atoms are sp2 hybridized? d. How many carbon, oxygen, and nitrogen atoms are sp3 hybridized? e. Does vitamin B6 exhibit delocalized bonding? Explain.arrow_forwardMethylcyanoacrylate is the active ingredient in super glues. Its Lewis structure is (a) Give values for the three bond angles indicated. (b) Indicate the most polar bond in the molecule. (c) Circle the shortest carbon-oxygen bond. (d) Circle the shortest carbon-carbon bond.arrow_forwardAspartame is an artificial sweetener marketed under the name Nutra-Sweet. A partial Lewis structure for aspartame is shown below. Aspartame can be classified as an organic compound (a compound based on carbon atoms). The majority of Lewis structures for simple organic compounds have all atoms with a formal charge of zero. Therefore, add lone pairs and multiple bonds to the structure above to give each atom a formal charge of zero when drawing the Lewis structure. Also note that the six-sided ring is shorthand notation for a benzene ring (C6H5). Benzene is discussed in Section 4-7. Complete the Lewis structure for aspartame. How many C and N atoms exhibit sp1 hybridization? How many C and O atoms exhibit sp3 hybridization? How many and bonds are in aspartame?arrow_forward
- Consider the molecule with the formula below, where X is the only central atom (all other atoms are directly bonded to X). Draw the most important Lewis structure for the molecule that follows the octet rule using the molecular charge and formal charges listed below. Determine the identity of X and the number of single and double bonds in your structure. Molecule formula: HXO2 Molecular charge: -1 Total number of valence electrons: 18 Formal charge on X: 0 The central atom (X) is: Click for List The molecule's number of single bonds is: The molecule's number of double bonds is: Click for List Click for Listarrow_forwardThe structure shown below is missing both its formal charges and lone pairs. Which of the choices correctly depicts the bond-line structure of this compound with correct formal charges? Incorrect Structure NEN NENO V=ル® NEN NENarrow_forwardWhat is the skeletal structure for the following molecule: (CH3)2C═CH(CH2)4CH3arrow_forward
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- How do you know when to draw a solid wedge vs a dashed wedge when drawing 3D bond-line structures? I know that solid-wedge means the atom is pointing towards you and dashed wedge means it's in the back, but how do you know which atoms are in the front as opposed to the back? How can you tell what the configuration will look like in space just by looking at the lewis structure or name?arrow_forwardGive the Expanded Lewis Structure and Bond Line Structure of the given compound. (kindly refer to the image below)arrow_forwardConsider the compound with the following condensed molecular formula: CH3CHOHCH=CH₂ What is the formal charge on the carbon atoms that only have single bonds? Formal charge: + What is the formal charge on the carbon atoms that have a double bond? Formal charge: + What is the formal charge on the oxygen atom? Formal charge: + What is the formal charge on the hydrogen atoms? Formal charge:arrow_forward
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INTRODUCTION TO MOLECULAR QUANTUM MECHANICS -Valence bond theory - 1; Author: AGK Chemistry;https://www.youtube.com/watch?v=U8kPBPqDIwM;License: Standard YouTube License, CC-BY