Draw all resonance forms for the following molecule
5. Arrange the following carbocations in order of decreasing stability. Draw ali possible resonance forms for each of them CH-cH-CHs+ CH CH+ CH3CH2+ CH-CH-CH-CH-CHt riate resonance Draw all resonance forms and a representation of the a hybrid for each of the foHowing s CH Rank the following six molecules in approximate order of decreasing Sl reactivity and decreasing Sx2 reactivity SN1 (decreasing->) Sw2 (decreasing→)
draw all resonance forms and a representation of the
appropriate resonance hybrid for each of the following
species
raw all resonand ail resonanu forms and a reesentahon of the appropi appropriate resonance hpbrid for each of tha Folwin species Indicale reso nan ce form that s major hat is major conhibub CH3 ら d) e)
Draw all significant resonance
forms. Do not draw resonance and curved arrows. Include formal
charges and lone pairs in your answer.
Question 1 CH3-C-CEN
7. Resonance in Organic Chemistry (22 points). A. Draw all the valid resonance forms of the ion below. At what sites can this ion react with a nucleophile? Indicate clearly with arrows.
3. For a) [CH3CH2C(-O)CH2l b) [CH3NHCHCHCH21 1) Draw their possible resonance forms as the Line-Angular structure. 2) Predict the product of the acid-base reaction between more stable resonance forms. Use the curved arrow to show the movement of electrons 3) Predict the product of the acid-base reaction between less stable resonance forms. 4) After comparing the reaction mechanisms and its products of 2) and 3). describe your opinion on the difference of stability of product.
3. For a) [CH3CH2C(-O)CH2l b)...
12. Draw the Lewis structure for the HTeO. ion, indicating any possible resonance forms. 3. Using VSEPR theory, predict and explain the molecular structures of Sn(NO,), and SeF
12. Draw the Lewis structure for the HTeO. ion, indicating any possible resonance forms. 3. Using VSEPR theory, predict and explain the molecular structures of Sn(NO,), and SeF
Four resonance structures of the following cation are possible. Two resonance forms are given below, but they are incomplete. Complete the given structures by adding nonbonding electrons and formal charges. Draw the two remaining resonance structures (in any order), including nonbonding electrons and formal charges HaC Ha H3 Which structure is the most stable (lowest energy) resonance contributor?
1. Draw all the resonance forms of the sigma complex formed by nitration of p-xylene.
1. For the following molecule, draw all possible reasonable resonance structures and then draw the corresponding resonance hybrid. Points will be deducted for invalid resonance structures (5 points) HO