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(a)
Interpretation:
Structural formula of the salt that is produced by reaction between propylamine and
Concept Introduction:
Neutralization reaction is the one that takes place between an acid and a base to give salt as product. As
(b)
Interpretation:
Structural formula of the salt that is produced by reaction between methylmethylamine and
Concept Introduction:
Neutralization reaction is the one that takes place between an acid and a base to give salt as product. As amines are bases due to the amino group in it, the reaction with inorganic acid or carboxylic acid gives salt as product. The salt formed is an amine salt. Proton is donated from the acid to the nitrogen atom which acts as a proton acceptor. In simple words, it can be said that in an amine‑acid reaction, the acid loses a hydrogen ion and amine gains a hydrogen ion.
(c)
Interpretation:
Structural formula of the salt that is produced by reaction between isobutylamine and
Concept Introduction:
Neutralization reaction is the one that takes place between an acid and a base to give salt as product. As amines are bases due to the amino group in it, the reaction with inorganic acid or carboxylic acid gives salt as product. The salt formed is an amine salt. Proton is donated from the acid to the nitrogen atom which acts as a proton acceptor. In simple words, it can be said that in an amine‑acid reaction, the acid loses a hydrogen ion and amine gains a hydrogen ion.
(d)
Interpretation:
Structural formula of the salt that is produced by reaction between cyclopentylethylamine and
Concept Introduction:
Neutralization reaction is the one that takes place between an acid and a base to give salt as product. As amines are bases due to the amino group in it, the reaction with inorganic acid or carboxylic acid gives salt as product. The salt formed is an amine salt. Proton is donated from the acid to the nitrogen atom which acts as a proton acceptor. In simple words, it can be said that in an amine‑acid reaction, the acid loses a hydrogen ion and amine gains a hydrogen ion.
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Chapter 17 Solutions
General, Organic, and Biological Chemistry
- option choice: Isoleucine Histidine Threonine Alanine Lysine Aspartate Tryptophan Tyrosine Leucine Arginine Cysteine Asparagine Valine Glutamine Glycine Methionine Serine Proline Phenylalanine Glutamatearrow_forwardsketch the nature of the metal-alkylidene bonding interactions.arrow_forwardPart C The perspective formula of isoleucine, an amino acid, is provided below. HOOC H₂NIC H 川 CH3 CH,CH3 Draw the Newman projection in staggered conformation for isoleucine by viewing the molecule along the C-2-C-3 bond. 1. Edit the Newman projection on the canvas. 2. Replace the appropriate hydrogens with the appropriate -CH3 or other groups. 3. If you need to start over, Undo or choose a Newman projection from the Templates toolbar (bottom). Important: Never delete the hydrogen atoms or bonds directly attached to the template, and do not move them by dragging or dropping them. That will break the projections structures. Only replace them! ▸ View Available Hint(s) 0 2 H± 3D EXP. L ד י CONT. 2 H 0 N оarrow_forward
- General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningOrganic 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
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
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