
Concept explainers
(a)
Interpretation:
The structure of 1-decanamine needs to be determined.
Concept Introduction:
The name of the
In the case of secondary and tertiary amines, if there are more than 1 same alkyl groups present, they are named using prefix di- or tri- along with the primary amine name. If there is more than one type of alkyl groups, they are named as N-substituted primary amines.
(b)
Interpretation:
The structure of tricyclohexylamine needs to be determined.
Concept Introduction:
The name of the amines is written based on their structure that whether they are primary, secondary or tertiary. The name of the primary amine is written using the longest carbon chain having the amine group. At the end of the name of the parent alkane chain, the suffix amine is added.
In the case of secondary and tertiary amines, if there are more than 1 same alkyl groups present, they are named using prefix di- or tri- along with the primary amine name. If there is more than one type of alkyl groups, they are named as N-substituted primary amines.
(c)
Interpretation:
The structure of p-bromoaniline needs to be determined.
Concept Introduction:
The name of the amines is written based on their structure that whether they are primary, secondary or tertiary. The name of the primary amine is written using the longest carbon chain having the amine group. At the end of the name of the parent alkane chain, the suffix amine is added.
In the case of secondary and tertiary amines, if there are more than 1 same alkyl groups present, they are named using prefix di- or tri- along with the primary amine name. If there is more than one type of alkyl groups, they are named as N-substituted primary amines.
(d)
Interpretation:
The structure of 3-aminobutanoic needs to be determined.
Concept Introduction:
The name of the amines is written based on their structure that whether they are primary, secondary or tertiary. The name of the primary amine is written using the longest carbon chain having the amine group. At the end of the name of the parent alkane chain, the suffix amine is added.
In the case of secondary and tertiary amines, if there are more than 1 same alkyl groups present, they are named using prefix di- or tri- along with the primary amine name. If there is more than one type of alkyl groups, they are named as N-substituted primary amines.
(e)
Interpretation:
The structure of N, N-dipropyl-2-octanmine needs to be determined.
Concept Introduction:
The name of the amines is written based on their structure that whether they are primary, secondary or tertiary. The name of the primary amine is written using the longest carbon chain having the amine group. At the end of the name of the parent alkane chain, the suffix amine is added.
In the case of secondary and tertiary amines, if there are more than 1 same alkyl groups present, they are named using prefix di- or tri- along with the primary amine name. If there is more than one type of alkyl groups, they are named as N-substituted primary amines.
(f)
Interpretation:
The structure of N-ethylhexylamine needs to be drawn.
Concept Introduction:
The name of the amines is written based on their structure that whether they are primary, secondary or tertiary. The name of the primary amine is written using the longest carbon chain having the amine group. At the end of the name of the parent alkane chain, the suffix amine is added.
In the case of secondary and tertiary amines, if there are more than 1 same alkyl groups present, they are named using prefix di- or tri- along with the primary amine name. If there is more than one type of alkyl groups, they are named as N-substituted primary amines.

Want to see the full answer?
Check out a sample textbook solution
Chapter 18 Solutions
General, Organic, & Biological Chemistry
- What is the final product when D-galactose reacts with hydroxylamine?arrow_forwardIndicate the formula of the product obtained by reacting methyl 5-chloro-5-oxopentanoate with 1 mole of 4-penten-1-ylmagnesium bromide.arrow_forwardIn the two chair conformations of glucose, the most stable is the one with all the OH groups in the equatorial position. Is this correct?arrow_forward
- please help me with my homeworkarrow_forwardhelparrow_forwardThe temperature on a sample of pure X held at 1.25 atm and -54. °C is increased until the sample boils. The temperature is then held constant and the pressure is decreased by 0.42 atm. On the phase diagram below draw a path that shows this set of changes. pressure (atm) 2 0 0 200 400 temperature (K) Xarrow_forward
- QUESTION: Answer Question 5: 'Calculating standard error of regression' STEP 1 by filling in all the empty green boxes *The values are all provided in the photo attached*arrow_forwardpressure (atm) 3 The pressure on a sample of pure X held at 47. °C and 0.88 atm is increased until the sample condenses. The pressure is then held constant and the temperature is decreased by 82. °C. On the phase diagram below draw a path that shows this set of changes. 0 0 200 temperature (K) 400 аarrow_forwarder your payment details | bar xb Home | bartleby x + aleksogi/x/isl.exe/1o u-lgNskr7j8P3jH-1Qs_pBanHhviTCeeBZbufuBYT0Hz7m7D3ZcW81NC1d8Kzb4srFik1OUFhKMUXzhGpw7k1 O States of Matter Sketching a described thermodynamic change on a phase diagram 0/5 The pressure on a sample of pure X held at 47. °C and 0.88 atm is increased until the sample condenses. The pressure is then held constant and the temperature is decreased by 82. °C. On the phase diagram below draw a path that shows this set of changes. pressure (atm) 1 3- 0- 0 200 Explanation Check temperature (K) 400 X Q Search L G 2025 McGraw Hill LLC. All Rights Reserved Terms of Use Privacy Cearrow_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





