Principles of General, Organic, Biological Chemistry
2nd Edition
ISBN: 9780073511191
Author: Janice Gorzynski Smith Dr.
Publisher: McGraw-Hill Education
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 10, Problem 10.54AP
Interpretation Introduction
Interpretation:
The complete structure of naproxen with all atoms and lone pairs has to be drawn.
Concept Introduction:
To draw a complete structure, the carbon has to be placed at the junction of each polygon. Then add enough hydrogen to form carbon four bonds. The lone pairs of electrons are present in heteroatom have to be drawn. The atom except carbon and hydrogen atom are known as heteroatom. The few examples of heteroatoms are nitrogen, oxygen and halogens
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
The structure of estrone, a female sex hormone, is shown below. Highlight and identify all of
the functional groups.
но
Estrone
Dihydroxyacetone (DHA), also known as glycerone, is the active ingredient in sunless tanning
products. DHA has the same molecular formula as glyceraldehyde, an important intermediate
in the metabolism of glucose. Highlight and label all the functional groups in DHA and
glyceraldehyde. What is the molecular formula for DHA and glyceraldehyde? What type of
isomers are DHA and glyceraldehyde?
OH
но,
HO,
LOH
DHA
Glyceraldehyde
Draw a complete structure for vanillin showing all C atoms, H atoms, and lone pairs. Vanillin is the
principal component of the extract of the vanilla bean.
но
-сно
vanillin
vanilla bean
Be sure to answer all parts.
Nonactin and valinomycin (shown below) each contain only two different types of functional groups.
nonactin
N.
H
valinomycin
Part 1 out of 2
What two functional groups are present in nonactin?
alkene
ester
alcohol
ether
エーZ
Chapter 10 Solutions
Principles of General, Organic, Biological Chemistry
Ch. 10.1 - Prob. 10.1PCh. 10.2 - Fill in all Hs and lone pairs in each compound. a....Ch. 10.3 - Convert each compound to a condensed formula.Ch. 10.3 - Convert each condensed formula to a complete...Ch. 10.3 - Convert each skeletal structure to a complete...Ch. 10.3 - How many Hs are bonded to each indicated carbon...Ch. 10.4 - Identify the functional groups in each compound....Ch. 10.4 - For each compound: [1] Identify the functional...Ch. 10.4 - Prob. 10.9PCh. 10.4 - Prob. 10.10P
Ch. 10.4 - Convert the ball-and-stick model of the local...Ch. 10.5 - How many hydrogen atoms are present in each...Ch. 10.5 - Prob. 10.13PCh. 10.5 - Prob. 10.14PCh. 10.5 - Prob. 10.15PCh. 10.5 - Prob. 10.16PCh. 10.6 - Give the IUPAC name for each compound.Ch. 10.6 - Prob. 10.18PCh. 10.6 - Prob. 10.19PCh. 10.6 - Prob. 10.20PCh. 10.7 - Prob. 10.21PCh. 10.7 - Prob. 10.22PCh. 10.9 - Answer the following questions about pentane...Ch. 10.9 - Prob. 10.24PCh. 10.9 - Prob. 10.25PCh. 10.10 - Prob. 10.26PCh. 10 - Prob. 10.27UKCCh. 10 - Prob. 10.28UKCCh. 10 - Prob. 10.29UKCCh. 10 - Prob. 10.30UKCCh. 10 - Prob. 10.31UKCCh. 10 - The largest known cycloalkane with a single ring...Ch. 10 - Draw three constitutional isomers having molecular...Ch. 10 - Draw four constitutional isomers having molecular...Ch. 10 - Answer the following questions about the alkane...Ch. 10 - Answer the questions in Problem 10.35 for the...Ch. 10 - Prob. 10.37UKCCh. 10 - Procaine (trade name Novocain) is a local...Ch. 10 - Prob. 10.39APCh. 10 - Prob. 10.40APCh. 10 - Complete each structure by filling in all Hs and...Ch. 10 - Prob. 10.42APCh. 10 - Prob. 10.43APCh. 10 - Prob. 10.44APCh. 10 - Prob. 10.45APCh. 10 - Prob. 10.46APCh. 10 - Convert each compound to a condensed structure.Ch. 10 - Prob. 10.48APCh. 10 - Prob. 10.49APCh. 10 - Prob. 10.50APCh. 10 - Prob. 10.51APCh. 10 - Prob. 10.52APCh. 10 - Albuterol (trade names: Proventil and Ventolin) is...Ch. 10 - Prob. 10.54APCh. 10 - Prob. 10.55APCh. 10 - Prob. 10.56APCh. 10 - Prob. 10.57APCh. 10 - Prob. 10.58APCh. 10 - Prob. 10.59APCh. 10 - Prob. 10.60APCh. 10 - Prob. 10.61APCh. 10 - Prob. 10.62APCh. 10 - Prob. 10.63APCh. 10 - Prob. 10.64APCh. 10 - Prob. 10.65APCh. 10 - Prob. 10.66APCh. 10 - Prob. 10.67APCh. 10 - Prob. 10.68APCh. 10 - Prob. 10.69APCh. 10 - Prob. 10.70APCh. 10 - Give the IUPAC name for each compound.Ch. 10 - Prob. 10.72APCh. 10 - Prob. 10.73APCh. 10 - Prob. 10.74APCh. 10 - Prob. 10.75APCh. 10 - Prob. 10.76APCh. 10 - Give the structure corresponding to each IUPAC...Ch. 10 - Prob. 10.78APCh. 10 - Prob. 10.79APCh. 10 - Each of the following IUPAC names is incorrect....Ch. 10 - Prob. 10.81APCh. 10 - Prob. 10.82APCh. 10 - Prob. 10.83APCh. 10 - Prob. 10.84APCh. 10 - Prob. 10.85APCh. 10 - Prob. 10.86APCh. 10 - Write a balanced equation for the incomplete...Ch. 10 - Prob. 10.88APCh. 10 - Prob. 10.89APCh. 10 - Prob. 10.90APCh. 10 - Prob. 10.91APCh. 10 - Prob. 10.92APCh. 10 - Answer the following questions for the cycloalkane...Ch. 10 - Prob. 10.94APCh. 10 - Prob. 10.95CPCh. 10 - Prob. 10.96CP
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- Why does hexane have the lower boiling point than acetic acid, when in fact, hexane has a high molecular mass? Boiling point determination can be used for several purposes. What are those purposes?arrow_forwardConsider lisinopril, a drug used primarily in the treatment of high blood pressure, heart failure, and after heart attacks. (a) Name the various functional groups in lisinopril. (b) What intermolecular forces are expected to exist between molecules of lisinopril in close proximity to one another (Section 5.7)?arrow_forwarddraw as a line bond structure of n-methylethanaminearrow_forward
- X. Circle and name each functional group in the following structure. H -OH cortisone acetate (active ingredient in steriod skin cream)arrow_forwardFollowing is the structure of cortisone, a corticosteroid that increases the blood glucose level and stimulates the synthesis of glycogen in the liver. What functional groups are in cortisone? Group of answer choices a. ketone group, aldehyde group, and carboxyl group, b.hydroxyl group, carboxyl group, and ether group c. hydroxyl group, ketone group, and alkene group d. ester group, amide group, and alkene grouparrow_forwardUse the following to answer the questions below: For each pair of compounds, select a con ct characterization from the response list. Responses may be used more than once or need not be used at all. a) have the same molecular formula but are different compounds b) both contain a carbon ring system c) contain the same number of carbon atoms but are not constitutional isomers d) two names for the same compound Methyl propanoate, Propyl methanoatearrow_forward
- draw 2 structural isomers for - structure b - structure e - structure farrow_forward7 8 9 Naltrexone is an FDA-approved treatment for alcoholism that targets the mu opioid receptor. Name four functional groups that are present in naltrexone. НО. OH amine, phenol, aldehyde, ether amine, phenol, amide, alcohol amine, phenol, ketone, alcohol ether, ketone, amide, alcohol ketone, phenol, alcohol, esterarrow_forwardIdentify and label all functional groups (alcohols, amines, amides, carboxylic acids, ketones, aldehydes, aromatic rings, aromatic amines, etc) of Carvone on the Lewis Structure. You do not have to circle alkanes. Make sure to add additional details about the functional groups of Carvonearrow_forward
- Match the circled groups to one of the following possible functional groups: ketone, aldehyde, amide, amine, carboxylic acid, ester, ether.arrow_forwardIdentify the functional groups in the ball-and-stick model of neral, a compound with a lemony odor isolated from lemongrass ?arrow_forwardIdentify the functional groups in the ball-and-stick model of elemicin, a compound partly responsible for the flavor and fragrance of nutmeg.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning
Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning
Organic And Biological Chemistry
Chemistry
ISBN:9781305081079
Author:STOKER, H. Stephen (howard Stephen)
Publisher:Cengage Learning,
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning
Alcohols, Ethers, and Epoxides: Crash Course Organic Chemistry #24; Author: Crash Course;https://www.youtube.com/watch?v=j04zMFwDeDU;License: Standard YouTube License, CC-BY