General, Organic, and Biological Chemistry - 4th edition
4th Edition
ISBN: 9781259883989
Author: by Janice Smith
Publisher: McGraw-Hill Education
expand_more
expand_more
format_list_bulleted
Videos
Textbook Question
Chapter 17.1, Problem 17.1P
Draw out each compound to clearly show what groups are bonded to the carbonyl carbon. Label each compound as a
a.
b.
c.
d.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Functional Group Classes
Alcohol
Amide
Ester
• CH₂CH₂OH
* CHIO-CH,
7. H₂C1O
Amine
Ketone
Circle each functional group(s) and identify the class to which each of the groups
belongs.
9. H₂C
Aldehyde
Thiol
Aromatics
Carboxylic Acid
2. CH,SH
6.
Alkenes
4. H₂NCH₂CH₂
10.
Ether
NM₂
11. Which of the functional groups in the top list must be on a terminalC in the carbon
chain?
1. Which functional group is found in aldehydes?
a. CHO
b. -CH;OH
c. -COOH
d. RCOR'
2. Which functional group is found in ketones?
a. -CHO
CH:OH
c. -COOH
RCOR'
3. Which structural feature is common to aldehydes and ketones?
a, an oxygen atom bonded to both a carbon atom and a hydrogen atom
b. an oxygen atom bonded to two carbon atoms
c. an oxygen atom double bonded to a carbon atom
d. two oxygen atoms bonded to the same carbon atom
4. What is the IUPAC name for the following compound?
a. I-pentaldehyde b. l-pentanal
c. pentanal
d. pentanealdehyde
Cetoa of Fi
What is the systematic IUPAC name for
the given compound?
CH3
CH3
CH;CHCH,CH,CH2
-Ń-CH3
a. N-methyl-4-methylhexan-1-amine
b. 2,4-dimethylhexan-1-amine
c. 2,2,N-trimethylpentan-1-amine
d. N,N,4-trimethylpentan-1-amine
Chapter 17 Solutions
General, Organic, and Biological Chemistry - 4th edition
Ch. 17.1 - Draw out each compound to clearly show what groups...Ch. 17.1 - Prob. 17.2PCh. 17.1 - (a) Label each functional group in lisinopril, a...Ch. 17.2 - Give the IUPAC name for each compound. a. b. c.Ch. 17.2 - Give the structure corresponding to each IUPAC...Ch. 17.2 - Prob. 17.5PCh. 17.2 - Give an acceptable name for each ester. a. CH3(...Ch. 17.2 - Prob. 17.6PCh. 17.2 - Prob. 17.7PCh. 17.2 - Prob. 17.8P
Ch. 17.2 - Prob. 17.9PCh. 17.3 - Which compound in each pair has the higher boiling...Ch. 17.4 - Prob. 17.11PCh. 17.5 - In addition to ethyl butanoate (Section 17.5),...Ch. 17.6 - Prob. 17.3PPCh. 17.6 - Prob. 17.13PCh. 17.6 - Which compound ¡n each pair ¡s more water soluble?...Ch. 17.6 - Prob. 17.5PPCh. 17.6 - Prob. 17.14PCh. 17.6 - Prob. 17.15PCh. 17.7 - Ibuprofen is another pain reliever that is a...Ch. 17.8 - Prob. 17.6PPCh. 17.8 - Prob. 17.17PCh. 17.8 - Prob. 17.18PCh. 17.8 - Prob. 17.7PPCh. 17.8 - Prob. 17.19PCh. 17.9 - Prob. 17.8PPCh. 17.9 - Prob. 17.20PCh. 17.9 - Prob. 17.21PCh. 17.9 - Prob. 17.22PCh. 17.9 - Prob. 17.9PPCh. 17.9 - Prob. 17.23PCh. 17.9 - Prob. 17.24PCh. 17.10 - Prob. 17.10PPCh. 17.10 - Prob. 17.25PCh. 17.11 - Prob. 17.26PCh. 17 - Prob. 27PCh. 17 - Prob. 28PCh. 17 - Prob. 29PCh. 17 - Prob. 30PCh. 17 - Prob. 31PCh. 17 - Prob. 32PCh. 17 - Prob. 33PCh. 17 - Prob. 34PCh. 17 - Prob. 35PCh. 17 - Give an acceptable name for each ester. a. CH3CO2(...Ch. 17 - Prob. 37PCh. 17 - Prob. 38PCh. 17 - Prob. 39PCh. 17 - Prob. 40PCh. 17 - Prob. 41PCh. 17 - Prob. 42PCh. 17 - Prob. 43PCh. 17 - Draw the structure corresponding to each name. a....Ch. 17 - Draw the structure corresponding to each name. a....Ch. 17 - Draw the structure corresponding to each name. a....Ch. 17 - Prob. 47PCh. 17 - Prob. 48PCh. 17 - Prob. 49PCh. 17 - Prob. 50PCh. 17 - Prob. 51PCh. 17 - Prob. 52PCh. 17 - Prob. 53PCh. 17 - Prob. 54PCh. 17 - What ester is formed when butanoic acid...Ch. 17 - Prob. 56PCh. 17 - Prob. 57PCh. 17 - Prob. 58PCh. 17 - Prob. 59PCh. 17 - Prob. 60PCh. 17 - Prob. 61PCh. 17 - Prob. 62PCh. 17 - Prob. 63PCh. 17 - Prob. 64PCh. 17 - Prob. 65PCh. 17 - Prob. 66PCh. 17 - What products are formed when each ester is...Ch. 17 - Prob. 68PCh. 17 - Prob. 69PCh. 17 - Prob. 70PCh. 17 - Prob. 71PCh. 17 - Prob. 72PCh. 17 - Prob. 73PCh. 17 - Prob. 74PCh. 17 - Draw the products formed in each reaction. a. b....Ch. 17 - Draw the products formed in each reaction. a. b....Ch. 17 - Answer the following questions about A, depicted...Ch. 17 - Answer the following questions about B, depicted...Ch. 17 - Prob. 79PCh. 17 - Prob. 80PCh. 17 - Prob. 81PCh. 17 - Prob. 82PCh. 17 - Prob. 83PCh. 17 - Prob. 84PCh. 17 - Prob. 85PCh. 17 - Prob. 86PCh. 17 - Prob. 87PCh. 17 - Prob. 88PCh. 17 - Prob. 89CPCh. 17 - Lactams can be hydrolyzed with base, just like...
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
- C Cont W k 1 ol Univ app.101edu.co Maps YouTube esc 1 Cont - F1 Q 9 A N Aktiv OH 2 Bb BIOC A X Univ Dr. HCC Sear Univ Bb BIO Mail Cont Question 1 of 19 What type of class of molecule is formed in the reaction illustrated here? A) aldehyde B) ketone C) ester + LOH Ht, heat D) carboxylate salt E) carboxylic acid F9 F2 W S X 1 H option command #m 3 80 F3 E D C $ 4 F4 R F do 5 % V F5 T G 6 MacBook Air F6 B Y H 7 N F7 U 8 J DII F8 M ( 9 Nath TPA G unive a Thar K O H O L F10 P F11 { + 11 I command option Do G self [ I ? F12 } ] + + Update Submit delete rearrow_forwardGive the IUPAC name of the following carboxylic acids and its derivatives.arrow_forwardsont HO OH Alcohol Carboxylic acid Amine C. Lone pairs and formal charges. OH H Amide Aldehyde Amine, Alcohol Carboxylic acidarrow_forward
- Acid anhydride Carboxylic Acid H₂C CH₂OH H₂O CH,OH CH3 Ester H₂C O CH₂OH 1. CH₂MgBr 2. H₂O* Acid chloride CH,CH,NH, Tertiary alcohol Amidearrow_forward8. Classify each alkene, alkyne., aromatic hydrocarbon, aleohol,ther ketone, carboxylic acidy Of the following organic compound as alkane , aldehyde amide, an hydrideor amine ester a. CHs CH z CH こ C4C4っ b. C. CH3 CHz CH - CH2O d. COCH3 e. CHz (cHz)8 C Hy f. CHz COO CHz CHz 9. cH, CH, CHz-CH h. CH EC - CHz Ctg i: CHz CH,-く4。 J. cH, C4 - と一6H K: CHs CH, NH CH> 1. CH3 - C-C Hz トH2 CH,arrow_forwardVancomycin is a useful antibiotic for treating infections in cancer patients on chemotherapy and renal patients on dialysis. How many amide functional groups are present in vancomycin? Which OH groups are bonded to sp3 hybridized carbon atoms and which are bonded to sp2 hybridized carbons?arrow_forward
- 2. Name the following carboxylic acids:arrow_forwardWhich molecule is an amide? a. CH 3 CH₂ CH₂ CH₂ C C. 0 0 b. || CH3 CH₂ CH₂N-C-CH₂-CH3 0 H CH3–CH2CH2CH2C-O-CH2-CH3 e. CH3CH2CH2NH2 d. CH 3 CH₂-CH₂-CH₂-CH₂-C 0 OHarrow_forwardErythronolide B is the biological precursor of erythromycin, a broad-spectrum antibiotic. What functional group Erythronolide B does contain? a. b. H₂CH₂C C. H₂C 1 H₂C 2 3 4 O Amide d. Amine OH Erythronolide B Ketone Aldehyde a CH₂ b C d CH₂ OH JCH₂ 'OH OHarrow_forward
- Sulfhydryl groupCarboxyl groupAmino groupHydroxy Brouparrow_forward15. It is believed that Alexander the Great was poisoned by an organic compound known as Strychnine. The structure of Strychnine is shown below. Identify the functional groups present in this molecule. a H "H b C --d A. a = tertiary amide, b = tertiary amine, c = alkene, d = ether B. a = ketone, b = secondary amine, c = alkene, d = ether C. a secondary amide, b = tertiary amine, c = alkyne, d = alcohol D. a = ketone, b = tertiary amide, c = alkyne, d = etherarrow_forward1. An amine is characterized by what functional group? a. -CO2CH3 b. -NH2 d. -CHO e. -OH c. -CO2H 2. Which of the follow ing is an akohol? a. NaOH d. CH CH 20OH b. H3CNH2 c. H3C-C-CH3 с. 3. When two alcohols undergo a self condensation, what is formed? a. liquid alcohol b. a ketone d. an aklehyde an ether e. с. an esterarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Introductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
Chemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
Chemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
Introductory Chemistry: A Foundation
Chemistry
ISBN:9781337399425
Author:Steven S. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning
07 Physical Properties of Organic Compounds; Author: Mindset;https://www.youtube.com/watch?v=UjlSgwq4w6U;License: Standard YouTube License, CC-BY