Concept explainers
(a)
Interpretation:
The structure of cyclobutylamine 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 of4-nonanamine 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 N-pentylaniline 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 of3-amino-2-butanone 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 of3-methyl-1-butanamine 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-ethyl-N-propylcyclopentylamine 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.
Want to see the full answer?
Check out a sample textbook solutionChapter 18 Solutions
GENERAL,ORGANIC, & BIOLOGICAL CHEM-ACCES
- Please correct answer and don't used hand raiting and don't used Ai solutionarrow_forwardPlease correct answer and don't used hand raitingarrow_forwardConsider the following Figure 2 and two atoms that are initially an infinite distance apart, x =00, at which point the potential energy of the system is U = 0. If they are brought together to x = x, the potential energy is related to the total force P by dU dx = P Given this, qualitatively sketch the variation of U with x. What happens at x=x? What is the significance of x = x, in terms of the potential energy? 0 P, Force 19 Attraction Total Repulsion x, Distance Figure 2. Variation with distance of the attractive, repulsive, and total forces between atoms. The slope dP/dx at the equilibrium spacing xe is proportional to the elastic modulus E; the stress σb, corresponding to the peak in total force, is the theoretical cohesive strength.arrow_forward
- Denote the dipole for the indicated bonds in the following molecules. H3C ✓ CH3 B F-CCl 3 Br-Cl H3C Si(CH3)3 wwwwwww OH НО. HO HO OH vitamin C CH3arrow_forwardFor the SN2 reaction, draw the major organic product and select the correct (R) or (S) designation around the stereocenter carbon in the organic substrate and organic product. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Η 1 D EN Select Draw Templates More C H D N Erasearrow_forwardQ9: Explain why compound I is protonated on O while compound II is protonated on N. NH2 NH2 I IIarrow_forward
- AN IR spectrum, a 13 CMR spectrum, and a 1 HMR spectrum were obtained for an unknown structure with a molecular formula of C9H10. Draw the structure of this compound.arrow_forwardAN IR spectrum, a 13 CMR spectrum, and a 1 HMR spectrum were obtained for an unknown structure with a molecular formula of C9H10. Draw the structure of this compound.arrow_forward(a) What is the hybridization of the carbon in the methyl cation (CH3*) and in the methyl anion (CH3¯)? (b) What is the approximate H-C-H bond angle in the methyl cation and in the methyl anion?arrow_forward
- Q8: Draw the resonance structures for the following molecule. Show the curved arrows (how you derive each resonance structure). Circle the major resonance contributor.arrow_forwardQ4: Draw the Lewis structures for the cyanate ion (OCN) and the fulminate ion (CNO). Draw all possible resonance structures for each. Determine which form for each is the major resonance contributor.arrow_forwardIn the following molecule, indicate the hybridization and shape of the indicated atoms. CH3 N CH3 HÖ: H3C CI: ::arrow_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