A) I B) II C) III D) IV E) V Identify the proper curved arrow to convert the first resonance structure into the second resonance structure. 1st || 2nd = ||| IV V
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- Place the following in order of decreasing dipole moment. |- CH4 II - CH3OH III - CH3SH III > | > || Il > | > II | > II| > | || > III > I | = II| > ||Please answer will surely given an upvote, thank youIn the molecule shown label the indicated bonds with either their hybridization (sp,sp2,sp3) or the type of bond present (sigma, pi )
- I 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.)10. Draw 2 valid resonance structures for each of the following molecule. a) b) c) : ZI H :0: :0: u N: the overall bybmultiple can be circled
- Please help me with both questiWhich of the following species is a valid resonance structure of A? Usecurved arrows to show how A is converted to any valid resonancestructure. When a compound is not a valid resonance structure of A,explain why not.Below is the SN2 reaction between iodocyclohexane and cyanide (CN–). Draw the missing curved arrow notation in the first box to reflect electron movements. In both boxes, add lone pairs of electrons and nonzero formal charges.
- Follow the curved arrows and draw a Lewis structure for the resulting resonance contributor of 1,3-butadiene, adding charges and lone electron pairs to the appropriate atoms. CH25.) Draw the important resonance forms for each of these. You do not have to draw in the curved arrows if you do not want to. a) b) c) +Please do all parts of the question