The first of the two heterolysis reactions below takes place readily, but the second one does not. Explain why. CH2 CI H3C H3C ECi-AI CI CI CI H3C H3C
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- Give the detailed mechanism for the following nitration reaction. Show the contributing resonance structures and the resonance hybrid for the intermediates. HNO,, H,SO, NO2Answer the question below the reaction. ta The reaction above proceeds through which type of mechanism? SN2 SN1 E1 E2 OH + Excess NH4C1 H₂SO4 + H₂OArrange the compounds below in order of increasing reactivity in a SN2 reaction. 1. (CH3)2СНCI 2. CH3CH2B1 3. CH3CH2C1 A) 1; 2; 3 В) 3;B 2; 1 C) 1; 3; 2 D) 2; 1; 3 E) 3; 1; 2
- Which of the following is most reactive under E2 conditions? Br Br Br Br (A) (B) (C) (D) O Compound B OCompound C Compound A Compound DIdentify the mechanisms by which each reactions above proceeds from the choices listed.What will be the major product of the following reaction and what is the likely mechanism for its formation? (CH;);COK Br racemic OCCCH3)3 OCCH3)3 ÓCCCH3)3 A B C D E
- 10. Draw the complete, detailed mechanism (curved arrows) for the following reaction, and predict the major product. CH3 ▪OH 1. DMSO (COCI)2 2. Et3N HFor each of the following reactions, state the mechanism the reaction will follow (E1,E2, SN1, SN2, etc.) and givethe major product(s) of the reaction.(c) The following reaction shows the electrophilic addition reaction between an alkene compound with hydrogen chloride, HCI. Tindak balas berikut menunjukkan tindak balas penambahan elektrofilik antara sebatian alkena dengan hidrogen klorida, HCI. + HCI Major product Draw the mechanism for the formation of major product. Lukis mekanisma bagi pembentukan hasil utama berikut.