Concept explainers
Interpretation:
The dash structural formula of DMF showing unshared electron pairs is to be drawn. The most important resonance form of DMF is to be predicted. On the basis of Lewis acid–base considerations, the greater reactivity of nucleophile in DMF is to be explained.
Concept introduction:
Electrophiles are electron-deficient species, which has positive or partially positive charge. Lewis acids are electrophiles, which accept electron pair.
Nucleophiles are electron-rich species, which has negative or partially negative charge. Lewis bases are nucleophiles, which donate electron pair.
In dash line formula, all the symbols of atoms and the bonding electron pair lines are shown.
Resonating structures are structures that have more than one equivalent Lewis structures for the same molecule or ion.
Resonance is the phenomenon of describing delocalized electrons in certain molecular ions through various forms or resonance structures and the forms contributing to the hybrid form.
The rules for drawing resonance structures are as follows:
Only nonbonding electron pairs and pi electrons can participate in conjugation in the formation of various resonating structures.
The single bonds present in the molecule do not break or form in the resonance structures.
The placement of atoms present in the molecule remains fixed.
The octet of all atoms is completely filled.
According to the convention, these structures are connected by double-headed arrows (
Movement of electrons (whether bonding or lone pair) is indicated by curved arrows.
Curved arrows are used to represent the direction of the flow of electrons in a reaction mechanism.
Curved arrows are drawn in such a way that they point from the source of an electron pair toward the atom, which receives the electron pair.
The direction of flow of electrons is always from a high electron density site to a low electron density site.
Curved arrows never represent the movement of atoms.
The movement of electrons shown by the curved arrows should not violate the octet rule for the elements, which are present in the second row of the periodic table.
The more stable structure is the structure that has more covalent bonds.
Stability of resonating structures is decreased by charge separation.
The structures that contain complete valence shells are more stable.
Reactivity of a molecule depends on the solvation of nucleophilic anions.
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Organic Chemistry
- The curved arrow notation introduced in Section 1.6B is a powerful method used by organic chemists to show the movement of electrons not 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 and formed in a reaction. Consider the following three-step process. (a) Add curved arrows in Step [1] to show the movement of electrons. (b) Use the curved arrows drawn in Step [2] to identify the structure of X. X is converted in Step [3] to phenol and HCl.arrow_forwardDraw electron dot and cross diagrams for the following compounds. Only the outermost shell of electrons needs to be shown. Use a different dot or cross for each atom or ion. (a) CH3COOH, ethanoic acid (b) S2Cl2, disulfur dichloride (c) O22, peroxide ion Provide everything stated in the instructions.arrow_forwardThe 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.arrow_forward
- Consider compounds A–D, which contain both a heteroatom and a double bond. (a) For which compounds are no additional Lewis structures possible? (b) When two or more Lewis structures can be drawn, draw all additional resonance structures.arrow_forwardDraw all of the resonance structures for each of the following species. Be sure to include the curved arrows that indicate which pairs of electrons are shifted in going from one resonance structure to the next. Draw the resonance hybrid of each species. (a) ОН (b) (c) H3Carrow_forwardFor each of the following pairs, use electronegativity differences to predict which compound has the higher boilingpoint.(a) MgBr2 or PBr3(b) OsO4 or SrO(c) Cl2O or Al2O3arrow_forward
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- Acetone [(CH3)2CO] is widely used as an industrial solvent.(a) Draw the Lewis structure for the acetone molecule andpredict the geometry around each carbon atom. (b) Is theacetone molecule polar or nonpolar? (c) What kinds ofintermolecular attractive forces exist between acetone molecules?(d) 1-Propanol (CH3CH2CH2OH) has a molecularweight that is very similar to that of acetone, yet acetoneboils at 56.5 °C and 1-propanol boils at 97.2 °C. Explain thedifference.arrow_forwardTrue or false: (a) The C¬C bonds in benzene are all the samelength and correspond to typical single C¬C bond lengths.(b) The C¬C bond in acetylene, HCCH, is longer than theaverage C¬C bond length in benzene.arrow_forwardwhat is the complete lewis structure of acetic anhydride such that all atoms have zero formal charge?arrow_forward
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