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Concept explainers
(a)
Interpretation:
Concept Introduction:
IUPAC rules for naming ammonium ions:
There are two rules that has to be followed while naming a positive ion (ammonium ion) and they are,
- In order to name an ammonium salt from alkylamine, the ending of the name
amine is changed from amine to ammonium ion. - In order to name an
aromatic amine, the ending of the name “-e” is replaced by “-ium ion”.
(b)
Interpretation:
Name of the amine salt has to be given.
Concept Introduction:
IUPAC rules for naming ammonium ions:
There are two rules that has to be followed while naming a positive ion (ammonium ion) and they are,
- In order to name an ammonium salt from alkylamine, the ending of the name amine is changed from amine to ammonium ion.
- In order to name an aromatic amine, the ending of the name “-e” is replaced by “-ium ion”.
(c)
Interpretation:
Name of the amine salt has to be given.
Concept Introduction:
IUPAC rules for naming ammonium ions:
There are two rules that has to be followed while naming a positive ion (ammonium ion) and they are,
- In order to name an ammonium salt from alkylamine, the ending of the name amine is changed from amine to ammonium ion.
- In order to name an aromatic amine, the ending of the name “-e” is replaced by “-ium ion”.
(d)
Interpretation:
Name of the amine salt has to be given.
Concept Introduction:
IUPAC rules for naming ammonium ions:
There are two rules that has to be followed while naming a positive ion (ammonium ion) and they are,
- In order to name an ammonium salt from alkylamine, the ending of the name amine is changed from amine to ammonium ion.
- In order to name an aromatic amine, the ending of the name “-e” is replaced by “-ium ion”.
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Chapter 17 Solutions
General, Organic, And Biological Chemistry, Hybrid (with Owlv2 Quick Prep For General Chemistry Printed Access Card)
- Nonearrow_forwardNonearrow_forwardWhat spectral features allow you to differentiate the product from the starting material? Use four separate paragraphs for each set of comparisons. You should have one paragraph each devoted to MS, HNMR, CNMR and IR. 2) For MS, the differing masses of molecular ions are a popular starting point. Including a unique fragmentation is important, too. 3) For HNMR, CNMR and IR state the peaks that are different and what makes them different (usually the presence or absence of certain groups). See if you can find two differences (in each set of IR, HNMR and CNMR spectra) due to the presence or absence of a functional group. Include peak locations. Alternatively, you can state a shift of a peak due to a change near a given functional group. Including peak locations for shifted peaks, as well as what these peaks are due to. Ideally, your focus should be on not just identifying the differences but explaining them in terms of functional group changes.arrow_forward
- Nonearrow_forwardNonearrow_forwardIn the solid state, oxalic acid occurs as a dihydrate with the formula H2C2O4 C+2H2O. Use this formula to calculate the formula weight of oxalic acid. Use the calculated formula weight and the number of moles (0.00504mol) of oxalic acid in each titrated unknown sample recorded in Table 6.4 to calculate the number of grams of pure oxalic acid dihydrate contained in each titrated unknown sample.arrow_forward
- 1. Consider a pair of elements with 2p and 4p valence orbitals (e.g., N and Se). Draw their (2p and 4p AO's) radial probability plots, and sketch their angular profiles. Then, consider these orbitals from the two atoms forming a homonuclear л-bond. Which element would have a stronger bond, and why? (4 points)arrow_forwardWrite the reaction and show the mechanism of the reaction. Include the mechanism for formation of the NO2+ 2. Explain, using resonance structures, why the meta isomer is formed. Draw possible resonance structures for ortho, meta and para.arrow_forwardNonearrow_forward
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