(a)
To determine: The test of the given hypothesis on the alkali metals; also the factors favoring the superoxide formation.
(a)

Answer to Problem 1DE
Solution: The oxidation of rubidium and cesium in presence of air forms superoxide. The bigger size of cation is a favorable factor for superoxide formation.
Explanation of Solution
The alkali metals such as rubidium and cesium which has lower first ionization energies can be used to test the given hypothesis. The larger size of cation results in the easy removal of electron due to which ionization energy of the atom decreases. Therefore, the oxidation of rubidium and cesium metal in presence of oxygen results in the formation of superoxide which confirms the statement that the lower ionization energy favors the superoxide formation.
The larger size cation can accommodate the larger size anion around it. Therefore, the bigger size of cation is a property which favors the superoxide formation.
The oxidation of rubidium and cesium in presence of air forms superoxide. The bigger size of cation is a favorable factor for superoxide formation.
(b)
To determine: The experiment to determine the potassium peroxide reacts with
(b)

Answer to Problem 1DE
Solution: The color of potassium superoxide salt changes from light yellow to white on reaction with water and carbon dioxide. The products of the reaction with water is
Explanation of Solution
The potassium superoxide is a yellow color salt. The reaction of potassium superoxide with water results in the change of its color from yellow to white. In the same way the potassium superoxide changes its color instaneously on coming in contact with water. This experiment confirms that the potassium superoxide reacts with carbon dioxide and water.
The reaction of potassium superoxide with water is given as,
The reaction of potassium superoxide with carbon dioxide is given as,
The color of potassium superoxide salt changes from light yellow to white on reaction with water and carbon dioxide. The products of the reaction with water is
(c)
To determine: The experiment to determine the reaction given in part (b) important in the firefighters breathing masks or not.
(c)

Answer to Problem 1DE
Solution: The green canister present in the breathing apparatus contains potassium superoxide as oxygen generator.
Explanation of Solution
The firefighter breathing apparatus contains a green canister which contains the chemicals which are used in the breathing apparatus. This is present at the base of the breathing device, The oxygen generated by the green canister is done by using potassium superoxide present in the green canister. This confirms that the reaction given in part (b) is important in the firefighters breathing apparatus.
The green canister present in the breathing apparatus contains potassium superoxide as oxygen generator.
(d)
To determine: The experiment to determine the percentages of
(d)

Answer to Problem 1DE
Solution: The reaction of
Explanation of Solution
The potassium superoxide on removal of oxygen at
The above reaction is still goes on heating will gives the formation of
After determining the mass of
The reaction of
Want to see more full solutions like this?
Chapter 7 Solutions
Laboratory Experiments For Chemistry: The Central Science, Si Edition
- Add conditions above and below the arrow that turn the reactant below into the product below in a single transformation. + More... If you need to write reagents above and below the arrow that have complex hydrocarbon groups in them, there is a set of standard abbreviations you can use. More... T H,N NC Datarrow_forwardIndicate the order of basicity of primary, secondary and tertiary amines.arrow_forward> Classify each of the following molecules as aromatic, antiaromatic, or nonaromatic. Cl Z- N O aromatic O antiaromatic O nonaromatic O aromatic O antiaromatic O nonaromatic O aromatic ○ antiaromatic nonaromaticarrow_forward
- Please help me answer this question. I don't understand how or even if this can happen in a single transformation. Please provide a detailed explanation and a drawing showing how it can happen in a single transformation. Add the necessary reagents and reaction conditions above and below the arrow in this organic reaction. If the products can't be made from the reactant with a single transformation, check the box under the drawing area instead.arrow_forward2) Draw the correct chemical structure (using line-angle drawings / "line structures") from their given IUPAC name: a. (E)-1-chloro-3,4,5-trimethylhex-2-ene b. (Z)-4,5,7-trimethyloct-4-en-2-ol C. (2E,6Z)-4-methylocta-2,6-dienearrow_forwardපිපිම Draw curved arrows to represent the flow of electrons in the reaction on the left Label the reactants on the left as either "Acid" or "Base" (iii) Decide which direction the equilibrium arrows will point in each reaction, based on the given pk, values (a) + H-O H 3-H + (c) H" H + H****H 000 44-00 NH₂ (e) i Дон OH Ө NHarrow_forward
- 3) Label the configuration in each of the following alkenes as E, Z, or N/A (for non-stereogenic centers). 00 E 000 N/A E Br N/A N/A (g) E N/A OH E (b) Oz N/A Br (d) 00 E Z N/A E (f) Oz N/A E (h) Z N/Aarrow_forward6) Fill in the missing Acid, pKa value, or conjugate base in the table below: Acid HCI Approximate pK, -7 Conjugate Base H-C: Hydronium (H₂O') -1.75 H-O-H Carboxylic Acids (RCOOH) Ammonium (NH4) 9.24 Water (H₂O) H-O-H Alcohols (ROH) RO-H Alkynes R--H Amines 25 25 38 HOarrow_forward5) Rank the following sets of compounds in order of decreasing acidity (most acidic to least acidic), and choose the justification(s) for each ranking. (a) OH V SH я вон CH most acidic (lowst pKa) least acidic (highest pKa) Effect(s) Effect(s) Effect(s) inductive effect O inductive effect O inductive effect electronegativity electronegativity O electronegativity resonance polarizability resonance polarizability O resonance O polarizability hybridization Ohybridization O hybridization оarrow_forward
- How negatively charged organic bases are formed.arrow_forwardNonearrow_forward1) For the following molecules: (i) Label the indicated alkenes as either cis (Z), trans (E), or N/A (for non-stereogenic centers) by bubbling in the appropriate label on the molecule. (ii) Complete the IUPAC name located below the structure (HINT: Put the letter of the configuration in parentheses at the beginning of the name!) E z N/A ()-3,4,6-trimethylhept-2-ene E Oz O N/A ()-3-ethyl-1-fluoro-4-methylhex-3-ene E -+- N/A Me )-2,3-dimethylpent-2-ene (d) (b) E O N/A Br ()-5-bromo-1-chloro-3-ethyloct-4-ene ОЕ Z N/A Et (___)-3-ethyl-4-methylhex-3-ene E (f) Oz N/A z N/A HO (4.7)-4-(2-hydroxyethyl)-7-methylnona-4,7-dien-2-onearrow_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





