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- 9) Suppose I want to perform a simple substitution reaction, replacing the OH with a Cl in the following compound. Which of the following reagents works best? Explain (and that means explain why the wrong answers are wrong as well as why the right answer is right). Option A: Addition of HBr Option B: Addition of SOC12/pyridine Option C: Addition of SOCl2 only OH ? J1Arrange 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; 2Answer the question below the reaction. ta The reaction above proceeds through which type of mechanism? SN2 SN1 E1 E2 OH + Excess NH4C1 H₂SO4 + H₂O
- Review topics] [References) 1. CI NaOH NH2 NaCI H20 2. OH NAHCO3 12 H20 CO2 Nal a = Proton transfer d = Electrophilic addition g = SN1 Nucleophilic substitution b = Lewis acid/base c = Radical chain substitution e = El Elimination h = SN2 Nucleophilic substitution f= E2 Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1. 2. Retry Entire Group 9 more group attempts remaining nswer[Review Topics] [References) In both series below the three aromatic compounds illustrated undergo the electrophilic substitution reaction shown NHČCH3 Reaction: Bromination Which compound (A, B, or C) reacts the fastest? Which compound (A, B, or C) reacts the slowest? C-H CH2CH2CH,CH3 Reaction: Chlorination Which compound (A, B, or C) reacts the fastest? Which compound (A, B, or C) reacts the slowest?ECinnamoyl chloride (C9H7CIOO) can be prepared by the two-step sequence shown below. Reaction 1: C7H60 + CAH6O3 C9H8O2 + C2H402 Reaction 2: C9H&O2 + SOC2 → C9H7oci + sO2 + HCI CH60 C4H6O3 C9H8O2 C2H402 SOCI2 C9H,Oci SO2 HCI Molar masses 106.12 102.09 148.16 60.05 118.96 166.60 64.07 36.46 (in g mol-1) What is the percent atom economy for the synthesis of cinnamoyl chloride? Enter an answer accurate to three significant figures. Number
- i need help filling out the following SN2 reactions with appopiate reactants, products, or reagents,myCoyote OWlv2 Homework Registration: CHEM 2... C OWLV2 | Online teaching and learning res.. * Start [Review Topics] [References) CH3 OMe H3C. CH3 MeOH CH3 CH3 CH3 H3C H3C H3C Br Alkyl halides undergo nucleophilic substitution and elimination reactions. When the kinetics of the reaction are measured, if the rate of the reaction is found to be dependent only upon the concentration of the alkyl halide the reaction is first order. The substitution reaction is thus termed SN1, and the elimination reaction is termed E1. These reactions are unimolecular and occur in two steps. The first step is rate-limiting and involves the loss of the leaving group to form a carbocation. In the second, fast, step the nucleophile adds to the carbocation in the SN1 reaction or elimination occurs to give an alkene in the E1 reaction. Because the carbocation is planar, the nucleophile can add to either face and therefore racemization is usually observed although solvent effects can influence this somewhat. E1…rank these from least to most reactive in nucleophilic acyl substitution with a nucleophile I)CH3COOC2H5 II) CH3COO-Na+ III)CH3COCl IV) CH3CONH2
- For the given molecule, highlight any nucleophilic sites in red and any electrophilic sites in blue. O: 439 0-HDecide which compounds from the list below are best suited for nucleophilic addition reactions and which ones are more appropriate for nucleophilic substitution reactions.For the reaction shown, the major products form via the A) SN1 B) SN2 C) E1 D) E2 H₂, Br CH3CH₂OLi ©2017 ProtonGuru.com E) Mixture of E1 and E2 F) Mixture of S1 and SN2 G) Mixture of Sn2 and E2 H) Mixture of S1 and E1 1) No reaction pathway(s).