(a)
Interpretation:
The symbol of the given name to be written.
Concept Introduction:
Naming monoatomic Ions:
Main group metal cations are named by identifying the metal name, followed by the word ‘ion’.
Naming
In general, transition metal exhibits various oxidation state and the naming follows the rule, transition metal is identified by the name, followed by the oxidation number of the particular ion.
Naming Anions:
Anions are named by replacing the end of the element name with ‘-ide’, followed by the word ‘ion’.
(b)
Interpretation:
Name of the given ion to be written.
Concept Introduction:
Naming monoatomic Ions:
Main group metal cations are named by identifying the metal name, followed by the word ‘ion’.
Naming Transition metal ion:
In general, transition metal exhibits various oxidation state and the naming follows the rule, transition metal is identified by the name, followed by the oxidation number of the particular ion.
Naming Anions:
Anions are named by replacing the end of the element name with ‘-ide’, followed by the word ‘ion’.
(c)
Interpretation:
Name of the given ion to be written.
Concept Introduction:
Naming monoatomic Ions:
Main group metal cations are named by identifying the metal name, followed by the word ‘ion’.
Naming Transition metal ion:
In general, transition metal exhibits various oxidation state and the naming follows the rule, transition metal is identified by the name, followed by the oxidation number of the particular ion.
Naming Anions:
Anions are named by replacing the end of the element name with ‘-ide’, followed by the word ‘ion’.
(d)
Interpretation:
Name of the given ion to be written.
Concept Introduction:
Naming monoatomic Ions:
Main group metal cations are named by identifying the metal name, followed by the word ‘ion’.
Naming Transition metal ion:
In general, transition metal exhibits various oxidation state and the naming follows the rule, transition metal is identified by the name, followed by the oxidation number of the particular ion.
Naming Anions:
Anions are named by replacing the end of the element name with ‘-ide’, followed by the word ‘ion’.
Want to see the full answer?
Check out a sample textbook solutionChapter 3 Solutions
FUND.OF GEN CHEM CHAP 1-13 W/ACCESS
- Draw the predominant form of glutamic acid at pH = 8.4. The pKa of the side chain is 4.1. Include proper stereochemistry. HO H2N OH pH = 8.4arrow_forwardHow would I draw this?arrow_forwardCalculate the standard change in Gibbs free energy, AGrxn, for the given reaction at 25.0 °C. Consult the table of thermodynamic properties for standard Gibbs free energy of formation values. NH,Cl(s) →NH; (aq) + C1 (aq) AGrxn -7.67 Correct Answer Determine the concentration of NH+ (aq) if the change in Gibbs free energy, AGrxn, for the reaction is -9.27 kJ/mol. 6.49 [NH+] Incorrect Answer kJ/mol Marrow_forward
- What are some topics of interest that neurotoxicologists study? For example, toxin-induced seizures, brain death, and such along those lines?arrow_forwardCould you help me with the explanation of the answer to exercise 15, chapter 1 of Lehinger Question Nombramiento de estereoisómeros con dos carbonos quirales utilizando el sistema RS(R,R)El isómero del metilfenidato (Ritalin) se utiliza para tratar el trastorno por déficit de atención con hiperactividad (TDAH).(S,S)El isómero es un antidepresivo. Identifique los dos carbonos quirales en la siguiente estructura. ¿Es este el(R,R)o el(S,S)¿isómero? Dibuja el otro isómero. Nombramiento de estereoisómeros con dos carbonos quirales utilizando el sistema RS(R,R)El isómero del metilfenidato (Ritalin) se utiliza para tratar el trastorno por déficit de atención con hiperactividad (TDAH).(S,S)El isómero es un antidepresivo.arrow_forwardThe reaction A+B → C + D AG°' = -7.3 kcal/mol can be coupled with which of the following unfavorable reactions to drive it forward? A. EFG+HAG° = 5.6 kcal/mol. B. J+KZ+A AG° = 2.3 kcal/mol. C. P+RY+DAG° = 8.2 kcal/mol. D. C + T → V + W AG°' = -5.9 kcal/mol. E. AN→ Q+KAG°' = 4.3 kcal/mol.arrow_forward
- What would be the toxicological endpoints for neurotoxicity?arrow_forwardWhat are "endpoints" in toxicology exactly? Please give an intuitive easy explanationarrow_forwardFura-2 Fluorescence (Arbitrary Unit) 4500 4000 3500 3000 2500 2000 1500 1000 500 [Ca2+]=2970nM, 25°C [Ca2+] 2970nM, 4°C [Ca2+]=0.9nM, 25°C [Ca2+] = 0.9nM, 4°C 0 260 280 300 340 360 380 400 420 440 Wavelength (nm) ← < The figure on the LHS shows the excitation spectra of Fura-2 (Em = 510 nm) in 2 solutions with two different Ca2+ ion concentration as indicated. Except for temperature, the setting for excitation & signal acquisition was identical.< ப a) The unit in Y-axis is arbitrary (unspecified). Why? < < b) Compare & contrast the excitation wavelength of the Isosbestic Point of Fura-2 at 25 °C & 4 °C. Give a possible reason for the discrepancy. < c) The fluorescence intensity at 25 °C & 4 °C are different. Explain why with the concept of electronic configuration. <arrow_forward
- Biology (MindTap Course List)BiologyISBN:9781337392938Author:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. BergPublisher:Cengage Learning
- Principles Of Radiographic Imaging: An Art And A ...Health & NutritionISBN:9781337711067Author:Richard R. Carlton, Arlene M. Adler, Vesna BalacPublisher:Cengage Learning