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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EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
- Draw the curved arrows to show the resonance structure for the following molecules. ( there are 3 molecules )arrow_forwardI dont understand. Select the bonds in the 3D representation of thymine below that are multiple bonds. (Hint: Consider the number of bonds attached to an atom in the image compared to the normal valence of that atom. In a valid structure, the number of bonds to an atom will equal the valence of that atom.)arrow_forwardx-xo B Draw molecule A. On that drawing include the lone pairs and the curved arrows that would produce resonance structure B.arrow_forward
- For 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_forwardBelow 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_forward
- Please do all parts of the questionarrow_forwardanswer 3 and 5. PLS MAKE IT LIKE THIS WAY SO THAT I UNDERSTAND IT IONIC YES OR NO POLAR YES OR NO NON POLAR YES OR NO IMF EXIST IS..... NO EXPLANATION NEEDED.arrow_forwardProblem (#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_forward
- The 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! ( answer with step by step explanation)arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning