It is the curved-arrow notation that shows how to attain one resonance structure from another. In other words, it shows how the electrons move in the structure of the compound. The movement of electrons always takes place in pairs. The electrons always move from tail to head as shown:
The tail must have the ability to donate electrons (lone pair or bond pair) and the head must have the ability to accept the electrons in accordance with the octet rule. The three possible movements for the curved arrow are:
Bond pair to lone pair
Lone pair to bond pair
Bond pair to bond pair
The formal charge also changes with each arrow by factor of 1. Since the tail donates the electrons, therefore it attains a positive charge. And since the head gains the electrons, therefore it attains a negative charge.
When a single Lewis structure is unable to represent the structure of a compound, then the resonance structures come into play. It is the movement of electrons that distinguish each resonance structure from the other.
The Lewis dot structure of is:
Another Lewis structure of obtained using the curved arrow-notation and showing the movement of electrons from to is:
The octet of carbon is not complete. Therefore, to complete the octet of , the lone pair on atom shifts to the atom thereby forming a new bond between the two.
Another Lewis structure obtained using the curved arrow-notation and showing the movement of -electrons from triple bond to is:
There will be a shift from -electrons of the triple bond to atom. Since the loses an electron and gains an electron, thus they get a neutral charge.
Finally, the curved arrow representation is:
Ans:The interconversion between the structures using the curved-arrow notation is:
The resonance structures of carbon monoxide are shown below. Show how each structure can be converted...
(a) Draw two resonance structures of the cation shown, shifting only one clectron pair in each step. Be sure to include the formal charge on structures B and C. Only move one double bond. Each resonance structure should contain only one charge -a positive charge. (b) Use curved-arrow notation on the given structure A to show its conversion to structure B, and then on structure B to show its conversion to structure C. 1. Draw curved arrows to show conversion of resonance...
(a) Draw two resonance structures of the cation shown below, shifting only one electron pair in each step. Be sure to include the formal charge on structures B and C.(b) Use curved-arrow notation on the given structure A to show its conversion to structure B, and then on structure B to show its conversion to structure C.
4. Three part problem. The structure shown below is stabilized by resonance. H a.) Redraw this structure to the left of the double headed arrow on your answer page. b.) Add one curved arrow to show how the second resonance form could be created. c.) Draw the second resonance form to the right of the double headed arrow. 5. The structure of the previous problem could react with water to form a hydrate. Draw the mechanism of hydrate formation. First,...
Part B The main resonance contributors of nitrobenzene are shown below. Use curved arrows to show how each contributor can be converted into the next. More than one arrow can be used per structure. You will need a total of four curved electron arrows to answer this question. H + N Edit the reaction by drawing all the required electron flow arrows. Electron flow arrows should start on an atom or a bond and should end on an atom, bond,...
EO 3- resonance structures, formal charges, stability 1. Draw ONE possible significant additional resonance structure for each of the following ions. Use curved arrows to show the movement of electrons that creates each new resonance structure. (Hint: lone pairs are not shown. Start by drawing in all one pairs, and include all lone pairs and formal charges in your additional resonance structure.) Page 1 of 3 2. For each structure, draw the resonance structure that is indicated by the curved...
Give all resonance structures for the following. Show how they interconvert using the curved arrow notation. We were unable to transcribe this image
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Draw reasonable resonance structures. Use electron pushing arrow notation to show the conversion of a resonance structure into another structure.
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Add curved arrows to show how the compound on the left is converted to the compound on the right. Squaric acid has a pKa of 1.5, making it much more acidic than many carboxylic acids (typical pKa values of 4-5). One of the reasons for its acidity is resonance stabilization of its conjugate base. which is shown below. Add curved arrows to the structure on the left to show how it is converted to the other resonance contributor shown to...