Concept explainers
Interpretation:
The Lewis diagrams for
Concept Introduction:
The Lewis structure shows the connectivity between atoms by identifying the lone pairs of electrons in a compound. Lewis structures are also known as Lewis dot structures. The valence electrons around an atom are shown by dots. Bonds between atoms are shown by lines and the lone pair of electrons is shown by a pair of dots.
Answer to Problem 77E
The Lewis diagrams for
The number of valence electrons present in
The Lewis diagrams for
Explanation of Solution
The number of valence electrons present in
The Lewis diagrams for
Figure 1
The two things that are alike about Lewis diagram for
• The number of valence electrons present in all species (
• The number of atoms attached to central metal atom in all species (
The Lewis diagrams for
Figure 2
The Lewis diagrams for
The number of valence electrons present in
The Lewis diagrams for
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Chapter 13 Solutions
EBK INTRODUCTORY CHEMISTRY: AN ACTIVE L
- 1. When hydrogen sulfide (H2S, MM = 34.08 g/mol) gas is bubbled into a solution of sodium hydroxide (NaOH, 40.00 g/mol), sodium sulfide (Na2S, 78.04 g/mol) and water (18.02 g/mol) are produced according to the balanced chemical equation shown below? H2S 2 NaOH --> Na2S 2 H₂O (a) Assuming the reaction goes to completion, how many grams of sodium sulfide are formed if 2.50g of hydrogen sulfide is bubbled into a solution containing 1.85g of NaOH? (20 pts) (b) Which reactant and how much of it remains after the reaction has been completed? (15 pts) (c) If only 0.400g of sodium sulfide was recovered, what is the percent yield of this reaction (5 pts)arrow_forwardThe organic compound MTBE (methyltertiarybutylether) is used as a fuel additive that allows gasoline to burn more cleanly thus leading to a reduction in pollution. Recently, however, MTBE has been found in the drinking water of a number of communities. As a result several states are phasing out the use of MTBE as a fuel additive. A combustion experiment using 10.00 g of MTBE was found to produce 24.97g of CO2 and 12.26 g of H2O. (a) What is the empirical formula of MTBE assuming it contains C, H, and O only? (b) The molar mass of MTBE was experimentally determined to be 88.1 g/mol. Using this information what is the molecular formula of MTBEarrow_forwardPart 4: Provide a detailed retrosynthetic analysis and a plausible forward synthesis the following molecule. храдо ofarrow_forward
- 3A: Starting with benzocyclobutene, synthesize the naphthalene derivative below.arrow_forward7. The addition of HBr to 2,5-dimethyl-2,4-heptadiene gives the same product, A, at both low and high temperatures. Provide the structure of A and explain the kinetic and thermodynamic product are the same in this reaction. HBr -78°C or 60°C Aarrow_forward3B: Convert the starting material into the chiral epoxytriol below. OH OH = OH OHarrow_forward
- 3D: Convert the aromatic triketone to the 1,3,5-triethylcyclohexane shown below. ہوئےarrow_forwardIndicate how to find the energy difference between two levels in cm-1, knowing that its value is 2.5x10-25 joules.arrow_forwardThe gyromagnetic ratio (gamma) for 1H is 2.675x108 s-1 T-1. If the applied field is 1,409 T what will be the separation between nuclear energy levels?arrow_forward
- Chances Ad ~stract one 11. (10pts total) Consider the radical chlorination of 1,3-diethylcyclohexane depicted below. 4 • 6H total $4th total Statistical pro 21 total 2 H A 2H 래 • 4H totul < 3°C-H werkest bund - abstraction he leads to then mo fac a) (6pts) How many unique mono-chlorinated products can be formed and what are the structures for the thermodynamically and statistically favored products? рос 6 -વા J Number of Unique Mono-Chlorinated Products Thermodynamically Favored Product Statistically Favored Product b) (4pts) Draw the arrow pushing mechanism for the FIRST propagation step (p-1) for the formation of the thermodynamically favored product. Only draw the p-1 step. You do not need to include lone pairs of electrons. No enthalpy calculation necessary H H-Clarrow_forwardWhat is the lone pair or charge that surrounds the nitrogen here to give it that negative charge?arrow_forwardLast Name, Firs Statifically more chances to abstract one of these 6H 11. (10pts total) Consider the radical chlorination of 1,3-diethylcyclohexane depicted below. 4 • 6H total $ 4th total 21 total 4H total ZH 2H Statistical H < 3°C-H werkst - product bund abstraction here leads to the mo favored a) (6pts) How many unique mono-chlorinated products can be formed and what are the structures for the thermodynamically and statistically favored products? Proclict 6 Number of Unique Mono-Chlorinated Products f Thermodynamically Favored Product Statistically Favored Product b) (4pts) Draw the arrow pushing mechanism for the FIRST propagation step (p-1) for the formation of the thermodynamically favored product. Only draw the p-1 step. You do not need to include lone pairs of electrons. No enthalpy calculation necessary 'H H-Cl Waterfoxarrow_forward
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