Concept explainers
(a)
Interpretation:
The orbital picture of methane indicating the important overlap of AOs is to be drawn.
Concept introduction:
According to
(b)
Interpretation:
The energy diagram of methane indicating the formation of molecular orbitals (MOs) is to be drawn.
Concept introduction:
The molecular orbitals are formed by overlapping of atomic orbitals of adjacent atoms. The number of molecular orbitals formed and the number of atomic orbitals that overlap is equal. The two atomic orbitals, on mixing along bonding axes, form two molecular orbitals: one is
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Organic Chemistry: Principles and Mechanisms (Second Edition)
- x-xo B Draw molecule A. On that drawing include the lone pairs and the curved arrows that would produce resonance structure B.arrow_forwardFor 1 and 2, use curved arrows to illustrate the potential overall electron movements or bond changes, and identify the type of reaction by examining the overall chemical transformation. Show A-H bonds as needed.arrow_forwardPlease write in image if possible and help me understand. I'm lostarrow_forward
- Below are two sets of resonance structures. Where applicable provide the missing curved arrow notation, lone pair electrons, and nonzero formal charge. Do not delete or add any bonds or atoms.arrow_forwardDescribe with words how you would draw the curved arrow(s) to get to the more stable resonance form for the left-hand pair. Be sure to include how many curved arrows are needed and what atom (or bond) the electrons are coming from or going to. Do the same for the resonance pair on the right-hand side. more stable more stablearrow_forwardPlease do all parts of the questionarrow_forward
- Problem (#2.) For each ion below, draw all reasonable resonance structures (linked by resonance arrows “↔”). Include curved arrows that indicate the movement of electrons between each resonance structure. Assign non-zero formal charges to each atom for each resonance structure. (a.) NO3– (nitrate) (b.) CH3COO– (acetate) (c.) N3– (azide) (d.) NCO– (isocyanate) Problem (#3.) For each ion in question 2, draw a resonance hybrid, assigning non-zero formal and/or partial charges (δ+, δ–) as needed. Problem (#4.) For each skeletal structure below, satisfy the valences (or octets) of all of the atoms by filling in double and triple bonds as well as unshared electron pairs. Assign non-zero formal charges and show the overall charge if the structure is an ion. See photo attached for Problem number 4. Problem (#5.) For each structure in question 4, draw a resonance hybrid (if it has one) and assign non-zero formal and/or partial charges as needed.arrow_forwardThe curved arrow notation introduced in Section 1.6 is a powerful method used by organic chemists to show the movement of electrons not only in resonance structures, but also in chemical reactions. Since each curved arrow shows the movement of two electrons, following the curved arrows illustrates what bonds are broken and formed in a reaction. Consider the following three-step process. (a) Add curved arrows in Step [1] to show the movement of electrons. (b) Use the curved arrows drawn in Step [2] to identify the structure of X. X is converted in Step [3] to phenol and HCl.arrow_forwardThe curved arrow notation introduced in Section 1.6 is a powerful method used by organic chemists to show the movement of electrons not only in resonance structures, but also in chemical reactions. Since each curved arrow shows the movement of two electrons, following the curved arrows illustrates what bonds are broken and formed in a reaction. Consider the following three-step process. (a) Add curved arrows in Step [1] to show the movement of electrons. (b) Use the curved arrows drawn in Step [2] to identify the structure of X. X is converted in Step [3] to phenol and HCl.arrow_forward
- See image belowarrow_forwardIdentify all functional groups that are present in strychnine, a highly toxic alkaloid used as a pesticide to kill rodents, whose line structure is shown here. What compound class is characteristic of each of those functional groups? Strychninearrow_forwardI am wondering why there is a need for resoance structures if the molecule already has a neutral charge. Wouldn't these all be insignificant resonance structures (as there is unnecessary charge separation)? Perhaps they are only depicting these structures for the purpose of showing high/low electron density (which was what the question was asking for)? 1 picture shows answer, another shows problem (it is (b)).arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning