Concept explainers
(a)
Interpretation:
All resonance contributors for sulfuric acid
Concept introduction:
If a species having two or more valid Lewis structures, then its resonance structure exists. Resonance structures are imaginary; true species is represented by the resonance hybrid. The resonance structures are differed by the placement of their valence electrons, and not their atoms. Resonance structures with a greater number of atoms having an octet complete, more covalent bonds, and fewer atoms having a non-zero formal charge are considered to be stable. While drawing resonance structures curved arrows are used. The movement of a pair of electrons is indicated by a curved arrow. A curved arrow originates from a lone pair of electrons or from a covalent double or triple bond to indicate the specific pair of electrons that are being moved. The arrow points to an atom if the electrons being moved become a lone pair. Otherwise, the arrow points to the center of an existing bond to represent the formation of a new double/triple bond. A resonance structure can be drawn if a lone pair of electrons on an atom is adjacent with multiple bonds or an incomplete octet on an atom is adjacent to multiple bonds or there is a ring of alternating single and multiple bonds.
(b)
Interpretation:
Resonance hybrid for
Concept introduction:
A resonance hybrid structure is a weighted average structure of all the resonance contributors. A partial bond is represented in a resonance hybrid by a dashed line connecting the two atoms. In the resonance hybrid, the partial bonds are shown, which represent the atoms over which the electrons are delocalized. The resonance hybrid structure looks most like the lowest energy resonance structure and it is the most stable structure. The more stable resonance structures have a) a greater number of atoms having octet complete, b) more number of covalent bonds, and c) fewer atoms having a non-zero formal charge.
(c)
Interpretation:
The resonance structures of
Concept introduction:
A resonance hybrid structure is a weighted average structure of all the resonance contributors. A partial bond is represented in a resonance hybrid by a dashed line connecting the two atoms. In the resonance hybrid, the partial bonds are shown, which represent the atoms over which the electrons are delocalized. The resonance hybrid structure looks most like the lowest energy resonance structure and it is the most stable structure. The more stable resonance structures have a) a greater number of atoms having octet complete, b) more number of covalent bonds, and c) fewer atoms having a non-zero formal charge.

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Chapter 1 Solutions
EBK GET READY FOR ORGANIC CHEMISTRY
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- Potential Energy (kJ) 1. Consider these three reactions as the elementary steps in the mechanism for a chemical reaction. AH = -950 kJ AH = 575 kJ (i) Cl₂ (g) + Pt (s) 2C1 (g) + Pt (s) Ea = 1550 kJ (ii) Cl (g)+ CO (g) + Pt (s) → CICO (g) + Pt (s) (iii) Cl (g) + CICO (g) → Cl₂CO (g) Ea = 2240 kJ Ea = 2350 kJ AH = -825 kJ 2600 2400 2200 2000 1800 1600 1400 1200 1000 a. Draw the potential energy diagram for the reaction. Label the data points for clarity. The potential energy of the reactants is 600 kJ 800 600 400 200 0 -200- -400 -600- -800- Reaction Progressarrow_forwardCan u help me figure out the reaction mechanisms for these, idk where to even startarrow_forwardHi, I need your help with the drawing, please. I have attached the question along with my lab instructions. Please use the reaction from the lab only, as we are not allowed to use outside sources. Thank you!arrow_forward
- Hi, I need your help i dont know which one to draw please. I’ve attached the question along with my lab instructions. Please use the reaction from the lab only, as we are not allowed to use outside sources. Thank you!arrow_forward5. Write the formation reaction of the following complex compounds from the following reactants: 6. AgNO₃ + K₂CrO₂ + NH₄OH → 7. HgNO₃ + excess KI → 8. Al(NO₃)₃ + excess NaOH →arrow_forwardIndicate whether the product formed in the reaction exhibits tautomerism. If so, draw the structure of the tautomers. CO₂C2H5 + CH3-NH-NH,arrow_forward
- Draw the major product of this reaction N-(cyclohex-1-en-1-yl)-1-(pyrrolidino) reacts with CH2=CHCHO, heat, H3O+arrow_forwardDraw the starting material that would be needed to make this product through an intramolecular Dieckmann reactionarrow_forwardDraw the major product of this reaction. Nitropropane reacts + pent-3-en-2-one reacts with NaOCH2CH3, CH3CHOHarrow_forward
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
