c. Compound A reacts with CH CI/AICI. CH2CV/AICI: 000 group directs the EAS The product of...
12 Identify the compound showing following infrared spectrum. 15 Identify the reaction CH, OH sequence for the following transformation CH (A) (B) CH,CI KMnO4H CH,COCI LAIHE AICI AICI Br2 CH3COCI HOCH CH OH Mg FeBry AICI H30* other CHỊ0 Hyo (A) (B) ОН (C) (D) Mg. Å CHCOCI H90 ОН Br2 (C) FeBly ether AICI (D) CH,COCI BEZ Mg CH2OH,0" AICI, FeBryother A factor which explains the large difference in the - boiling point of OCH OH 13 following two...
6) What is the product of the following reaction? 1. CHECHE *CI AICI: 2. H₂O A) CH.CH; B) CH.CH.CH ОН Сң CH.CH D) CH-CH2 CHE E) CH-CH:CH OH
1. Write the predicted product and the rate law for the following reaction: CH;CH CH CI + NaCN DMSO 2. In the following reaction, identify a) the leaving group, b) the nucleophile, c) the electrophilic carbon and d) the solvent CH CH Br + NaHS H30 CH CH SH + NaBr 3. Write out the reaction of (R)-2-bromopentane with sodium cyanide in DMSO, including the predicted major product: 4. Rank the following in decreasing order of leaving group ability (with...
please help.me with these pls CH, CH, C-Cl + CHÁNH, The major product of this reaction is (C) (D) (A) (B) 1 NCH; CH CHUC-Cl 0 CH, CH,C-NHCH, ch,ch,ccu,NE, CH, CHC-C1 NHCH, 0 CH, C OH (1) + CH OH 2 CH, C 0 CH + H2O After protonation, the mechanism of this reaction starts with attack (A) (1) because the carboxylic acid is more acidic than the alcohol. (B) (1) because the carboxylic acid is a better nucleophile than...
What isare) the product(s) of the following reaction? CH + CHECH,CH,CI Alch CH,CH(CH, a mixture of C.H.CH.CH,CH, and CH.CH(CH)2 CH.CH.CH.CH C.H.CH,CH.CH,C1 Where would the compound shown below undergo bromination with NBS and benzoyl peroxide? meta position on ring 1 C(2) position on ring 2 ortho/para position on ring 1 methyl group on ring 2 Which of the following aromatic compounds reacts faster than benzene in electrophilic aromatic bromination? Which of the following is the best method to make n-butylbenzene? A)...
identify the compound showing infrared spectrum 12 Identify the compound showing following infrared spectrum. CH OH 15 Identify the reaction sequence for the following transformation. Trance CH berom (A) ОН (A) CHCI KMnO4. H* CH3COCI LIAH, AICI AICI B) Br2 CH3COC! HOCH2CH2OH Mg FeBry AICI H30* ether CH,0 но* Br2 Mg & CHCOCI H90 (C) FeBr ether AICI CH,COCI BI? Mg CH20 H30 AICI FeBrzether (C) (D) ОН (D) 13 Identify the major product of 16 following reaction. HO CH,...
2. Compound A reacts with E+ to form the ortho and meta intermediates shown below. ENN Orice om contato M1 M2 The least stable intermediate is ___, which tells me the CN group is a director. Check two (2) boxes. N 01 (blank 1) O O 02 (blank 1) 03 (blank 1) 04 (blank 1) M1 (blank 1) M2 (blank 1) M3 (blank 1) M4 (blank 1) O ortho, para (blank 2) O meta (blank 2)
pppppplllleeeaaassseee help 1. a. Compound 1 reacts with A under acid conditions to form an imine. What could Z be in this reaction? b. Compound 2 reacts with A (same A as previous reaction) under acid conditions to form an amide. What is Z in this reaction? Draw the structure of A Use curved arrows to show how Compound 2 forms the amide. c. Both reactions involve a leaving group. What is the leaving group in each reaction? O A...
Draw the product of the following reaction: CI 1. AICI: 2. H20 O
Question 11 (2 points) Choose a major product for the reaction below. Cl2/AICI: OCH3 CI OCH3 OCH3 HI OCH3 HI 1 O a) 11 Ob) III O c) I, II and III Od)! Question 12 (2 points) Predict the structure of the major product for the following reaction. CH3CH2CCI Zn (Hg) CHCI AICI NH2 11 III IV O a) IV Ob) III Oc) O d) II