Concept explainers
(a)
Interpretation:
Structural formula for the parent amine from which the substituted ammonium ion is formed has to be drawn.
Concept Introduction:
Substituted ammonium ion is the one in which one or more alkyl, aryl, or cycloalkyl groups are substituted instead of hydrogen atoms. There are two important generalizations that is applied to the substituted ammonium ion and they are,
- Substituted ammonium ions are not neutral molecules. They are charged species.
- Nitrogen atom has four bonds in ammonium ion or substituted ammonium ion. The species is positively charged as the fourth bond formed is a coordinate covalent bond.
(b)
Interpretation:
Structural formula for the parent amine from which the substituted ammonium ion is formed has to be drawn.
Concept Introduction:
Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.
Substituted ammonium ion is the one in which one or more alkyl, aryl, or cycloalkyl groups are substituted instead of hydrogen atoms. There are two important generalizations that is applied to the substituted ammonium ion and they are,
- Substituted ammonium ions are not neutral molecules. They are charged species.
- Nitrogen atom has four bonds in ammonium ion or substituted ammonium ion. The species is positively charged as the fourth bond formed is a coordinate covalent bond.
(c)
Interpretation:
Structural formula for the parent amine from which the substituted anilinium ion is formed has to be drawn.
Concept Introduction:
Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.
Substituted ammonium ion is the one in which one or more alkyl, aryl, or cycloalkyl groups are substituted instead of hydrogen atoms. There are two important generalizations that is applied to the substituted ammonium ion and they are,
- Substituted ammonium ions are not neutral molecules. They are charged species.
- Nitrogen atom has four bonds in ammonium ion or substituted ammonium ion. The species is positively charged as the fourth bond formed is a coordinate covalent bond.
(d)
Interpretation:
Structural formula for the parent amine from which the substituted anilinium ion is formed has to be drawn.
Concept Introduction:
Amines are a class of organic compounds. They are derivatives of ammonia. Similar to the nitrogen atom in ammonia, the amine nitrogen also has a lone pair of electrons on it. This means that amines can act as proton acceptors. When an amine is added to water a proton is transferred to the nitrogen atom. The resulting solution is a basic solution. This contains ammonium ions and hydroxide ions.
Substituted ammonium ion is the one in which one or more alkyl, aryl, or cycloalkyl groups are substituted instead of hydrogen atoms. There are two important generalizations that is applied to the substituted ammonium ion and they are,
- Substituted ammonium ions are not neutral molecules. They are charged species.
- Nitrogen atom has four bonds in ammonium ion or substituted ammonium ion. The species is positively charged as the fourth bond formed is a coordinate covalent bond.
Want to see the full answer?
Check out a sample textbook solutionChapter 17 Solutions
Bundle: General, Organic, and Biological Chemistry, 7th + OWLv2 Quick Prep for General Chemistry, 4 terms (24 months) Printed Access Card
- 3. You may want to read paragraph 1.5 in your textbook before answering this question. Give electron configuration (short-hand notation is fine) for: (5 points) 3+ a) Manganese atom and Mn³+ b) Se atom c) Cu atom and Cu+arrow_forwardPlease correct answer and don't use hand ratingarrow_forwardNonearrow_forward
- Nonearrow_forwardHowever, why are intermolecular forces in metallic and ionic compounds not discussed as extensively? Additionally, what specific types of intermolecular attractions exist in metals and ionic compoundsarrow_forwardWhat is the preparation of 1 Liter of 0.1M NH4Cl buffer at pH 9.0 with solid NH4Cl and 0.1M NaOH. How would I calculate the math to describe this preparation? How would I use Henderson-Hasselbach equation?arrow_forward
- C Predict the major products of this organic reaction. Be sure you use wedge and dash bonds when necessary, for example to distinguish between major products with different stereochemistry. : ☐ + x G C RCO₂H Click and drag to start drawing a structure.arrow_forwardFill in the blanks by selecting the appropriate term from below: For a process that is non-spontaneous and that favors products at equilibrium, we know that a) ΔrG∘ΔrG∘ _________, b) ΔunivSΔunivS _________, c) ΔsysSΔsysS _________, and d) ΔrH∘ΔrH∘ _________.arrow_forwardHighest occupied molecular orbital Lowest unoccupied molecular orbital Label all nodes and regions of highest and lowest electron density for both orbitals.arrow_forward
- Relative Intensity Part VI. consider the multi-step reaction below for compounds A, B, and C. These compounds were subjected to mass spectrometric analysis and the following spectra for A, B, and C was obtained. Draw the structure of B and C and match all three compounds to the correct spectra. Relative Intensity Relative Intensity 20 NaоH 0103 Br (B) H2504 → (c) (A) 100- MS-NU-0547 80 40 20 31 10 20 100- MS2016-05353CM 80 60 100 MS-NJ-09-3 80 60 40 20 45 J.L 80 S1 84 M+ absent राग 135 137 S2 62 164 166 11 S3 25 50 75 100 125 150 175 m/zarrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forwardDon't used hand raitingarrow_forward
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningChemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub Co
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning