![World of Chemistry, 3rd edition](https://www.bartleby.com/isbn_cover_images/9781133109655/9781133109655_smallCoverImage.jpg)
Concept explainers
(a)
Interpretation:
The systematic name of given compound is to be written.
Concept introduction:
The compounds are named as per IUPAC rules.
To name a compound, general pattern which is used is:
Prefix + word-root + suffix
(a)
![Check Mark](/static/check-mark.png)
Answer to Problem 55A
3-Methylbutanoic acid
Explanation of Solution
The numbering is done from right side to give carboxylic group number 1. ‘oic acid’ suffix is used to indicate carboxylic group.
The chain contains four carbon atoms which are single bonded. So word-root ‘butan’ is used. ‘e’ is removed as per the rules.
The skeleton shows one methyl is attached at C-3. Therefore, name of compound is 3-Methylbutanoic acid
(b)
Interpretation:
The systematic name of given compound is to be written.
Concept introduction:
The compounds are named as per IUPAC rules.
To name a compound, general pattern which is used is:
Prefix + word-root + suffix
(b)
![Check Mark](/static/check-mark.png)
Answer to Problem 55A
Benzenecarboxylic acid
Explanation of Solution
(c)
Interpretation:
The systematic name of given compound is to be written.
Concept introduction:
The compounds are named as per IUPAC rules.
To name a compound, general pattern which is used is:
Prefix + word-root + suffix
(c)
![Check Mark](/static/check-mark.png)
Answer to Problem 55A
2-Hydroxypropanoic acid
Explanation of Solution
The numbering is done from right side to give carboxylic group number 1. ‘oic acid’ suffix is used to indicate carboxylic group.
The chain contains three carbon atoms which are single bonded. So word-root ‘propan’ is used. ‘e’ is removed as per the rules.
The skeleton shows one hydroxyl is attached at C-2. Therefore, name of compound is2-Hydroxypropanoic acid
(d)
Interpretation:
The systematic name of given compound is to be written.
Concept introduction:
The compounds are named as per IUPAC rules.
To name a compound, general pattern which is used is:
Prefix + word-root + suffix
(d)
![Check Mark](/static/check-mark.png)
Answer to Problem 55A
3,4-Dimethylhexanoic acid
Explanation of Solution
The numbering is done from right side to give carboxylic group number 1. ‘oic acid’ suffix is used to indicate carboxylic group.
The chain contains six carbon atoms which are single bonded. So word-root ‘hexan’ is used. ‘e’ is removed as per the rules.
The skeleton shows two methyl groups are attached one at C-3 and other at C-4. Therefore, name of compound is 3,4-Dimethylhexanoic acid
Chapter 20 Solutions
World of Chemistry, 3rd edition
- H2SO4 (cat.), H₂O 100 °C NH₂arrow_forwardX Draw the major products of the elimination reaction below. If elimination would not occur at a significant rate, check the box under the drawing area instead. ది www. Cl + OH Elimination will not occur at a significant rate. Click and drag to start drawing a structure.arrow_forwardNonearrow_forward
- 1A H 2A Li Be Use the References to access important values if needed for this question. 8A 3A 4A 5A 6A 7A He B C N O F Ne Na Mg 3B 4B 5B 6B 7B 8B-1B 2B Al Si P 1B 2B Al Si P S Cl Ar K Ca Sc Ti V Cr Mn Fe Co Ni Cu Zn Ga Ge As Se Br Kr Rb Sr Y Zr Nb Mo Tc Ru Rh Pd Ag Cd In Sn Sb Te I Xe * Cs Ba La Hf Ta W Re Os Ir Pt Au Hg Tl Pb Bi Po At Rn Fr Ra Ac Rf Ha ****** Ce Pr Nd Pm Sm Eu Gd Tb Dy Ho Er Tm Yb Lu Th Pa U Np Pu Am Cm Bk Cf Es Fm Md No Lr Analyze the following reaction by looking at the electron configurations given below each box. Put a number and a symbol in each box to show the number and kind of the corresponding atom or ion. Use the smallest integers possible. cation anion + + Shell 1: 2 Shell 2: 8 Shell 3: 1 Shell 1 : 2 Shell 2 : 6 Shell 1 : 2 Shell 2: 8 Shell 1: 2 Shell 2: 8arrow_forwardNonearrow_forwardIV. Show the detailed synthesis strategy for the following compounds. a. CH3CH2CH2CH2Br CH3CH2CCH2CH2CH3arrow_forward
- Do the electrons on the OH participate in resonance with the ring through a p orbital? How many pi electrons are in the ring, 4 (from the two double bonds) or 6 (including the electrons on the O)?arrow_forwardPredict and draw the product of the following organic reaction:arrow_forwardNonearrow_forward
- Redraw the molecule below as a skeletal ("line") structure. Be sure to use wedge and dash bonds if necessary to accurately represent the direction of the bonds to ring substituents. Cl. Br Click and drag to start drawing a structure. : ☐ ☑ Parrow_forwardK m Choose the best reagents to complete the following reaction. L ZI 0 Problem 4 of 11 A 1. NaOH 2. CH3CH2CH2NH2 1. HCI B OH 2. CH3CH2CH2NH2 DII F1 F2 F3 F4 F5 A F6 C CH3CH2CH2NH2 1. SOCl2 D 2. CH3CH2CH2NH2 1. CH3CH2CH2NH2 E 2. SOCl2 Done PrtScn Home End FA FQ 510 * PgUp M Submit PgDn F11arrow_forwardNonearrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780078021558/9780078021558_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781118431221/9781118431221_smallCoverImage.gif)