Interpretation:
The wedge-dashed wedge-line formulas of both A and B are to be drawn and the change in configuration is to be determined.
Concept introduction:
Reaction sequences involve conversion of one
These sequences involve a number of steps carried out by different reagents. Sometimes different reagents give the same products.
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.
Substitution reaction: A reaction in which one of the hydrogen atoms of a hydrocarbon or a functional group is substituted by any other functional group is called substitution reaction.
Nucleophilic substitution reaction is a reaction in which an electron-rich nucleophile attacks the positive or partial positive charge of an atom or a group of atoms to replace a leaving group.
An
An
The involvement of nearby nucleophile substituent to the reaction center in the substitution process is known as neighboring group participation.
Such participation results in an increase of
In this participation, two
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Organic Chemistry
- 3. Predict the products of the following reactions. When more than one product is expected, predict which will be the major product? ОН H,SO4 H;PO4 (a) (b) heat OH heat CH3 Br CH3 Br NaOCH3 NaOC(CH3)3 (c) (d)arrow_forward(i) State reagents G and J. (ii) Draw the structural formula for compounds D, E and H.arrow_forward1. At what position and on what ring would you expect the following substances to undergo electrophilic substitution? (b) CH3 Br lel CH3 2. Rank the compounds in each group according to their reactivity toward electrophilic substitution. (a) Chlorobenzene, o-dichlorobenzene, benzene (b) p-Bromonitrobenzene, nitrobenzene, phenol (c) Fluorobenzene, benzaldehyde, 0-xylene (d) Benzonitrile, p-methylbenzonitrile, p-methoxybenzonitrilearrow_forward
- Provide the starting materials needed to prepare the following compounds:arrow_forward5) Show how cross Claisen condensations could be used to prepare the following: (b) Ph-CH-C-OCH, (a) Ph-č-CH-C-OCH,CH, С-с-осн, ĆH,arrow_forward1.(a) Which of the following groups has the LOWEST IUPAC priority?(A) CH3 (B) NH2 (C) OH (D) COOH (E) Br (b)Which of the following corresponds to the strongest acid?(A) (CF3)3C-COOH (B) (CF3)3 C-OH(C) CH3COOH (D) CH3OH(E) HOCH2CH3arrow_forward
- Give reasons for the following: (i) p-nitrophenol is more acidic than p-methylphenol. (ii) Bond length of C—O bond in phenol is shorter than that in methanol. (iii) (CH3)3C—Br on reaction with sodium methoxide (Na+ _OCH3) gives alkene as the main product and not an ether.arrow_forwardB: complete the following reactions (а) Br CH3 HC1 СОН CH3 (b) HOCH2CH, heat CH2CH2OH + 2HB1arrow_forwardProvide the structure of the product(s) with stereochemisty if appropriate. If multiple products indicate major product or if products are formed in equal amounts. If there is no reaction expected explain why. (a) OH HIO4 (the protecting group is remained) CHO H HOH2C OH (b) CHO -ОН NaCN # HO -H H -OH CH₂OH (c) CHO HO- -H HO -H NH₂OH 張一 H -OH H -OH CH₂OH i) Ba(OH)2 ii) MeOH, H₂SO4 NaOAc Ac₂0 NaOMe MeOHarrow_forward
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