Concept explainers
(a)
Interpretation:
The compound has to be matched with appropriate
Concept introduction:
Resonance effect:
Organic compound contains double bonds, it will involve in the overlap of p-orbitals on the two adjacent carbon atoms.
Inductive effect:
The electronic effect arises due to the polarisation of σ bonds within a molecule and it is due to an electronegativity difference between the atoms.
(b)
Interpretation:
The compound has to be matched with appropriate
Concept introduction:
Resonance effect:
Organic compound contains double bonds, it will involve in the overlap of p-orbitals on the two adjacent carbon atoms.
Inductive effect:
The electronic effect arises due to the polarisation of σ bonds within a molecule and it is due to an electronegativity difference between the atoms.
(c)
Interpretation:
The compound has to be matched with appropriate
Concept introduction:
Resonance effect:
Organic compound contains double bonds, it will involve in the overlap of p-orbitals on the two adjacent carbon atoms.
Inductive effect:
The electronic effect arises due to the polarisation of σ bonds within a molecule and it is due to an electronegativity difference between the atoms.
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Chapter 21 Solutions
Student Study Guide and Solutions Manual for Brown/Iverson/Anslyn/Foote's Organic Chemistry, 8th Edition
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- (a) Give an acceptable name for each compound, (b) Draw the organic products formed when A or B is treated with each reagent: [1] H3O+; [2] −OH, H2O; [3] CH3CH2CH2MgBr (excess), then H2O; [4] LiAlH4, then H2O.arrow_forwardThe hydrocarbon fluorene was treated with potassium t-butoxide in an acid-base reaction, giving the fluorenide anion and t-butyl alcohol. (a) Which way does the equilibrium lie, and by how much? b) What is the proportion of the fluorenide anion to fluorene? (c) Why is fluorene so highly acidic, considering the pKa of an average alkane is above 50?arrow_forwardGive reasons: (i) Bond length of C = O in carboxylic acids is slightly larger than C = O bond length in carbonyl compounds. (ii) There are two –NH2 groups in semicarbazide. However, only one –NH2 group is involved in the formation of semicarbazones. (iii) Benzoic acid is less soluble in water than acetic acid. (iv) Formic acid is a stronger acid than acetic acid.arrow_forward
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- Why are carboxylic acids more acidic than alcohols? The increased inductive effect of the alkyl group of the carboxylic acid resonance stabilization of the carboxylate ion (conjugate base of carboxylic acids) Due to hydrogen bonding They have high pKa valuesarrow_forwardWhich of the following bases is strong enough to deprotonate N,Ndimethylacetamide [CH3CON(CH3)2, pKa = 30], so that equilibrium favors the products: (a) NaNH2; (b) NaOH?arrow_forward4) Multistriatin, one of the pheremones of the elm bark beetle, is a volatile compound released by a virgin female beetle when she has found a good food source - an elm tree. Male beetles, which carry the Dutch elm disease fungus, are attracted by the pheromone; the tree becomes infected with the fungus and soon dies. Multistriatin is used to trap the beetles, but the amount in beetles is so miniscule that the compound must be synthesized. The following synthesis of multistriatin uses only chemistry that we have seen in Chem 348. HO. НО Br type O type. H type H H CH3 H HO HO type O H CH3 "Η OH type H hint: anhydrous cond CH3 H = H type type HO CH3 H H type CH 3 H Multistriatin Multistriatinarrow_forward
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