Write the net ionic reactions and designate the nucleophile, substrate and the leaving group in the following reactions. CH3 CH3OCH2CH3 CH3CH2ONa + Nal a) 2CH3OH (CH3)3CCI b) (CH3)3 COCH3 CH3OH 2 + CI Br + 2NH3 c) NH2 + NH4Br
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- What is the product of the reaction of ethyl bromide with each of the following nucleophiles? CH3CH2CH2O- CH3C≡C- (CH3)3NThe number of different monochlorinated constitutional isomers produced when each of the following undergo a uv light catalysed reaction with chlorine: Compound i: 2 Compound: ii: 1 Compound i: 3 Compound: ii: 4 Compound i: 4 Compound: ii: 2 Compound i: 5 Compound: ii: 1 Compound i: 6 Compound: ii: 3Alcohols are acidic in nature. Therefore, a strong base can abstract the acidic hydrogen atom of the alcohol in a process known as deprotonation. The alcohol forms an alkoxide ion by losing the proton attached to the oxygen atom of the hydroxyl ( -OH) group. The alkoxide formed can act as a base or a nucleophile depending on the substrate and reaction conditions. However, not all bases can abstract the acidic proton of alcohols and not all alcohols easily lose the proton. Deprotonation depends on the strength of the base and the acidity of the alcohol. Strong bases, such as NaNH2, can easily abstract a proton from almost all alcohols. Likewise, more acidic alcohols lose a proton more easily. Determine which of the following reactions would undergo deprotonation based on the strength of the base and the acidity of the alcohol. Check all that apply. ► View Available Hint(s) CH3CH,OH + NH3 →CH,CH,O-NH CH3 CH3 H3C-C-H+NH3 → H3 C-C-H OH O-NH CH3CH2OH + NaNH, → CH3CH,O-Na* + NH3 CHC12 Cl₂…
- Identify the leaving group for a potential elimination of the following compounds. Compare the leaving group activities for A and K. Which of the following compounds cannot be subjected to elimination? Explain.Do not give handwriting solution.What reaction category/mechanism type does the following reaction fit? O addition substitution (SN1) substitution (SN2) O elimination (E1) O elimination (E2) HCI CI + HO
- 102. The major products A and B in the following reaction sequence are CHO Br Br (i) PPh3 (ii) NaH (A) NaH OH (B)Rank the nucleophiles in following group in order of increasing nucleophilicity. H2O, −OH, CH3CO2-Answer the question below the reaction. O4S H3C H3C H3C OH In the first step of the reaction mechanism, which of the following is formed? CH3 H3C CH3 CH3 + Excess NH4Cl OH CH3 (+) -OH2 CH 3 CH3 OH CH3 H₂SO₁ CH3 CI ха +H2O
- Select the major intermediate in the chlorination (Cl2/AlCl3) of benzoic acid. COOH бас -CI COOH A Ос ОВ OA OD O None COOH В C COOH D сWhich of the following species is the least nucleophilic? HO (CH3)3CO H₂O (CH3)3N CNWrite the structure of the organic compound (Alkyne) that gives these products on ozonolysis: