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- Organic chemistry is a bit like cooking. Later in this course we will study “recipes” for preparingnew molecules. A common instruction in such recipes is “add a strong acid” or “add a strongbase” (rarely are they added at the same time since a violent reaction ensues). You will see theseterms frequently from now on, and are expected to be able to recognize them or draw theirstructures from memory. Memorize them before next class.3) Combine any Atomic orbitals to form Molecular orbitals assuming they fulfill the phase and energy requirement. Construct MO diagram (include AOs, MOs, pictures of each, electrons, HOMO, LUMO, B.O., and comparative energies, etc.). REMOVE an ELECTRON to form CATION Please only do part 3. The first image shows the problemDraw a bond-line structure that best matches the given 3D representation?
- Statement 1: The boiling point of compound2 is lower because of the number of bondingregions present Statement 2: Moreover the increased no. of sigmabonds result to more difficult distortion resulting to a stronger attractive force within the atoms prensent Which is true? Statement 1, 2, both, or noneA student argues the the two nitrogen’s in the compound below are sp2 hybridized, but atom a is still more basic than atom b. Is the student correct? Explain.Give typed explanation Which of the indicated position(s) in the molecule below would likely react with a positively charged atom? A and B only A only D only A and D only
- Chemistry is it the one on the right becuae the reaonance structure of the conj base is more delocalized/stable than the conj base of the left? can you draw a resonance of both so i can check my work? thanks guysPlease draw the arrow formalism on the 1st structure (top) that accounts for the 2nd resonance structure (bottom).Polarity (a 3-d representation with bond and molecular dipoles annotated) of ClO4- , PF3, H2O, PF5 , SF4
- a.Determine the number of nodes and rank them in order of increasing energy. b.Draw the p atomic orbital contributions on each carbon atom (AO mixing pattern) that would give rise to the MO. c. Based on your answer to part (c) -determine whether each MO is overall bonding, nonbonding, or antibonding. Please explain stepsPolarity (a 3-d representation with bond and molecular dipoles annotated) of HCN, BeF2, SO2, O3, OF2, BF3Help,please provide explanation! (a) Draw the orbital picture for diazomethane (shown below) showing the explicit overlap of the contributing AO's. (b) Draw the MO energy diagram for diazomethane and identify the HOMO and LUMO.