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(a)
Interpretation:The resonance structures of bicarbonate ion needs to be drawn with the use of electron pushing arrows and the form that will be the major contributor to the real structure of bicarbonate ion needs to be determined.
Concept Introduction:VSEPR theory stands as Valence Shell Electron Pair Repulsion Theory. It helps to predict the molecular shape or geometry of the molecule with the help of the number of bond pair or lone pair present in it. According to VSEPR theory, the presence of lone pair on the central atom of molecule causes deviation from standard molecular geometry.
The resonance is the phenomenon in which if all the properties cannot explain by one structure, it can be shown in two or more structures by the shifting of pi bonds or lone pair but there is no change in sigma bond and position of atoms.
(b)
Interpretation:The resonance structures of
Concept Introduction:VSEPR theory stands as Valence Shell Electron Pair Repulsion Theory. It helps to predict the molecular shape or geometry of the molecule with the help of the number of bond pair or lone pair present in it. According to VSEPR theory, the presence of lone pair on the central atom of molecule causes deviation from standard molecular geometry.
The resonance is the phenomenon in which if all the properties cannot explain by one structure, it can be shown in two or more structures by the shifting of pi bonds or lone pair but there is no change in sigma bond and position of atoms.
(c)
Interpretation:The resonance structures of
Concept Introduction:VSEPR theory stands as Valence Shell Electron Pair Repulsion Theory. It helps to predict the molecular shape or geometry of the molecule with the help of the number of bond pair or lone pair present in it. According to VSEPR theory, the presence of lone pair on the central atom of molecule causes deviation from standard molecular geometry.
The resonance is the phenomenon in which if all the properties cannot explain by one structure, it can be shown in two or more structures by the shifting of pi bonds or lone pair but there is no change in sigma bond and position of atoms.
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Chapter 1 Solutions
Organic Chemistry: Structure and Function
- Predict the major products of this organic reaction: H OH 1. LiAlH4 2. H₂O ? Note: be sure you use dash and wedge bonds when necessary, for example to distinguish between major products with different stereochemistry. Click and drag to start drawing a structure. G C टेarrow_forwardFor each reaction below, decide if the first stable organic product that forms in solution will create a new C-C bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. NH2 CI MgCl ? Will the first product that forms in this reaction create a new CC bond? Yes No MgBr ? Will the first product that forms in this reaction create a new CC bond? Yes No G टेarrow_forwardFor each reaction below, decide if the first stable organic product that forms in solution will create a new CC bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. དྲ。 ✗MgBr ? O CI Will the first product that forms in this reaction create a new C-C bond? Yes No • ? Will the first product that forms in this reaction create a new CC bond? Yes No × : ☐ Xarrow_forward
- Predict the major products of this organic reaction: OH NaBH4 H ? CH3OH Note: be sure you use dash and wedge bonds when necessary, for example to distinguish between major products with different stereochemistry. Click and drag to start drawing a structure. ☐ : Sarrow_forwardPredict the major products of this organic reaction: 1. LIAIHA 2. H₂O ? Note: be sure you use dash and wedge bonds when necessary, for example to distinguish between major products with different stereochemistry. Click and drag to start drawing a structure. X : ☐arrow_forwardFor each reaction below, decide if the first stable organic product that forms in solution will create a new C - C bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. NH2 tu ? ? OH Will the first product that forms in this reaction create a new CC bond? Yes No Will the first product that forms in this reaction create a new CC bond? Yes No C $ ©arrow_forward
- As the lead product manager at OrganometALEKS Industries, you are trying to decide if the following reaction will make a molecule with a new C-C bond as its major product: 1. MgCl ? 2. H₂O* If this reaction will work, draw the major organic product or products you would expect in the drawing area below. If there's more than one major product, you can draw them in any arrangement you like. Be sure you use wedge and dash bonds if necessary, for example to distinguish between major products with different stereochemistry. If the major products of this reaction won't have a new CC bond, just check the box under the drawing area and leave it blank. Click and drag to start drawing a structure. This reaction will not make a product with a new CC bond. G marrow_forwardIncluding activity coefficients, find [Hg22+] in saturated Hg2Br2 in 0.00100 M NH4 Ksp Hg2Br2 = 5.6×10-23.arrow_forwardgive example for the following(by equation) a. Converting a water insoluble compound to a soluble one. b. Diazotization reaction form diazonium salt c. coupling reaction of a diazonium salt d. indacator properties of MO e. Diazotization ( diazonium salt of bromobenzene)arrow_forward
- 2-Propanone and ethyllithium are mixed and subsequently acid hydrolyzed. Draw and name the structures of the products.arrow_forward(Methanesulfinyl)methane is reacted with NaH, and then with acetophenone. Draw and name the structures of the products.arrow_forward3-Oxo-butanenitrile and (E)-2-butenal are mixed with sodium ethoxide in ethanol. Draw and name the structures of the products.arrow_forward
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