write out the SN1 reaction, showing both products, of 2-chlorobutane in 50/50 ethanol/water.
Reaction equations for each of the following with silver nitrate in ethanol (SN1): - 2-Chlorobutane -2-bromobutane - Bromobenzene - 2-Bromo- 2-methylpropane
What would be the leaving group if 2-Chlorobutane reacts with AgNO3 in an Sn1 reaction? Also What would be the leaving group if 1-Bromobutane reacts with AgNO3 in an Sn1 reaction?
insert the product structure for the reactions AgNO3+ Ethanol (SN1) (Write product structure below) Compound HC 1-Chlorobutane CH HC 2-Chlorobutane CH3 HC 2-Bromobutane Br HC 1-Bromobutane CH3 HC- CI CHE t-butylchloride Benzylchloride Bromobenzene
which reaction is faster and why ? (0.1 ml 2-Chlorobutane and 1% ethanolic silver nitrate solution) or (0.1 ml 2-Chlorobutane and silver nitrate in a mixture of 50% ethanol-50% water)
2. Three separate reactions are conducted as outlined below. Reaction 1: 4 drops of 1-chlorobutane in 2 mL of 1% AgNO, in ethanol. Reaction 2: 4 drops of 2-chlorobutane in 2 mL of 1% AgNO, in ethanol. Reaction 3:4 drops of t-butyl chloride in 2 mL of 1% AgNO, in ethanol. a. List the expected rate of each of the reactions. List the slowest reaction first and fastest reaction last. b. Explain your reasoning based on substrate structure, the nature...
1. arrange Alkyl chlorides in theoretical order of reactivity in SN1 reaction 2. arrange Alkyl chlorides in theoretical order of reactivity in SN2 reaction a HC 1-Chlorobutane AgNO3+ Ethanol (SN1) Nal + Acetone SN2 CH3 H3C 2-Chlorobutane Br CH3 H3C 2-Bromobutane CH3 H2C- a CH3 t-butylchloride Benzylchloride Br Bromobenzene
please answer all parts Does 1-chlorobutane, an alkyl chloride, undergo a substitution reaction with the nucleophiles NaCl, NaBr, or Nal? Solubility data for each of these nucleophiles and the substrate is given in Table 1 below. Table 1: Solubility of Compounds in Various Solvents Compound Solvents in Which Soluble 1-chlorobutane Diethyl ether, hexanes, acetone, tetrahydrofuran NaCl Water, glycerol, ethylene glycol, formic acid NaBr Water, methanol Nal Water, ethanol, acetone 4. Write balanced chemical equations showing 1-chlorobutane undergoing a nucleophilic substitution...
please answer all parts Does 1-chlorobutane, an alkyl chloride, undergo a substitution reaction with the nucleophiles NaCl, NaBr, or Nal? Solubility data for each of these nucleophiles and the substrate is given in Table 1 below. Table 1: Solubility of Compounds in Various Solvents Compound Solvents in Which Soluble 1-chlorobutane Diethyl ether, hexanes, acetone, tetrahydrofuran NaCl Water, glycerol, ethylene glycol, formic acid NaBr Water, methanol Nal Water, ethanol, acetone 4. Write balanced chemical equations showing 1-chlorobutane undergoing a nucleophilic substitution...
Write the potential sn2 and sn1 reaction as well as the potential the sn2 and sn1 mechanism. Then state which reaction(s) will occur if any, and why? with naI/acetone and with AgNO3/ethanol F) chlorobenzene G) 1-bromobutane H) 2-bromobutane
Write the potential sn2 and sn1 reaction as well as the potential the sn2 and sn1 mechanism. Then state which reaction(s) will occur if any, and why? with NaI/acetone and AgNO3 and ethanol C) 2-iodobutane D) t-butyl chloride E) benzyl chloride