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- Draw the missing lone-pair electrons and assign the missing formal charge on N or O for the following H-C-O-HUse the formal charge to draw in the lone pairs on each N or O atom in the following compounds.Draw the Lewis structure (including all lone pair electrons and any formal charges) for one of the four possible isomers of C3H9N.
- Projection drawings of all isomers of C6H4Cl2. Can you convert one into another without breaking any bonds? What type of isomerism do these represent?How many π bonds are there in 1,2-propadiene (H-C=C=C-H)?draw the full lewis structures of a ketone isomer and an aldehyde isomer with the formula C6H6O . make sure lone pairs are shown ketone aldehyde
- Write the best Lewis or Kekulé structure (showing all lone pairs of electrons, formal charges, and appropriate geometry – use wedge-dash where needed) for each of the following species given as condensed formulas: a) NH2- b) PO3H3 c) H2COH+ d) NaBH3CN e) C6H5MgBr f) CH3AlCl2Draw thee other resonance structures for the following carbocation. Use electron pushing arrows in order to derive one resonance structure from another. Indicate the formal charge on each atom in your structures.The curved arrow notation introduced in Section 1.6B is a powerfulmethod used by organic chemists to show the movement of electronsnot only in resonance structures, but also in chemical reactions.Because each curved arrow shows the movement of two electrons,following the curved arrows illustrates what bonds are broken andformed in a reaction. Consider the following three-step process. (a) Addcurved arrows in Step [1] to show the movement of electrons. (b) Use thecurved arrows drawn in Step [2] to identify the structure of X. X isconverted in Step [3] to phenol and HCl.