Concept explainers
(a)
Interpretation:
Given equation has to be balanced.
(a)
Explanation of Solution
Given equation is,
The oxidation state of manganese has changed from
Balancing the equation:
Balanced chemical equation can be written for the given reaction by the method of half-reactions. Summing up the half-reactions obtained gives the resultant reaction.
Therefore, the balanced chemical equation is,
(b)
Interpretation:
Amount of bromide ions that is required to produce
(b)
Explanation of Solution
In the problem statement it is given that the yield is
Therefore, the amount of bromide ions required is
(c)
Interpretation:
The mass of manganese dioxide that is required to produce
(c)
Explanation of Solution
In the problem statement it is given that the yield is
Therefore, the amount of manganese dioxide required is
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Chapter 19 Solutions
Chemistry: The Molecular Science
- SH 0arrow_forward2. Please consider the two all 'cis' isomers of trimethylcyclohexane drawn below. Draw the two chair conformers of each stereoisomer below (1 and 2) and calculate their torsional interaction energies in order to identify the lower energy conformer for each stereoisomer. Based on your calculations, state which of the two stereoisomers 1 and 2 is less stable and which is more stable. [1,3-diaxial CH3 CH3 = 3.7kcal/mol; 1,3-diaxial CH3 H = 0.88kcal/mol; cis-1,2 (axial:equatorial) CH3 CH3 = 0.88kcal/mol; trans-1,2-diequatorial CH3 CH3 = 0.88kcal/mol) all-cis-1,2,3- 1 all-cis-1,2,4- 2arrow_forwardNonearrow_forward
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- Describe the principle of resonance and give a set of Lewis Structures to illustrate your explanation.arrow_forwardDon't used hand raitingarrow_forwardIt is not unexpected that the methoxyl substituent on a cyclohexane ring prefers to adopt the equatorial conformation. OMe H A G₂ = +0.6 kcal/mol OMe What is unexpected is that the closely related 2-methoxytetrahydropyran prefers the axial conformation: H H OMe OMe A Gp=-0.6 kcal/mol Methoxy: CH3O group Please be specific and clearly write the reason why this is observed. This effect that provides stabilization of the axial OCH 3 group in this molecule is called the anomeric effect. [Recall in the way of example, the staggered conformer of ethane is more stable than eclipsed owing to bonding MO interacting with anti-bonding MO...]arrow_forward
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