Can you explain with all necessary steps and equations? thank you 1. Butyl chloride, CH,CI, reacts...
1. Butyl chloride, C.H.CI, reacts with water to form butyl alcohol, C.H.OH. CH,Cl (aq) + H2O (1) - C.H.OH(aq) + HCl(aq) If the initial concentration of butyl chloride is 0.1000 M and the concentration after 50 s of reaction is 0.0905 M, calculate the average rate of reaction (at the start of the reaction, i.e., the initial rate).
Can you explain with all necessary steps and equations? thank you 4. Use the method of initial rates (the simple method, not the more robust approach) to determine the rate law and rate constant for the reaction NH + NO3 - N2 + 2 H2O (acid solution) Given the following data: [HNO2]/M [NH *] / M. Rate x 108/mol Li's! 0.0092 0.098 34.9 0.0092 0.049 16.6 0.0488 0.196 335 0.0249 0.196 156
Can you explain with all necessary steps and equations? thank you 6. The reaction 2 H2 + 2 NO N2 + 2 H20 may proceed by the following mechanism: 2 NO - N202 (k, and k.1) H2 + N202 N2O + H2O (kz) H + N20 - N2 + H2O (ku). Use the steady-state approximation to predict the rate law for the formation of the product N.
The hydrolysis of tert-butyl chloride occurs according to the following equation and rate law: C4H9Cl + H2O C4H9OH + HCl rate = k[C4H9Cl] Starting with an initial concentration [C4H9Cl] = 0.10 M, the concentration reached 0.05 M after 342 seconds at a temperature of 308K. What is the rate constant under these conditions? 2. The hydrolysis of tert-butyl chloride occurs according to the following equation and rate law: C&HgCl + H2O + C4H,OH + HCI rate = k[C4H9CI] Starting...
Can you please explain with all steps and necessary equations? Thank you! 6. The force constant of the CO group in a peptide link is approximately 1.2 kN m'. At what wavenumber would you expect it to absorb? Treat the CO subunit as a separate molecule to find the reduced mass.
please help with questions 1 and 2.. thank you! 1. A reaction in a kinetics experiment is started when 4.00 mL of 0.100 M t-butyl chloride is mixed with solvent (diluted) to a final volume of 20.0 mL. After 65 sec, t1/no has been reached. a. What is the concentration of t-butyl chloride (molarity) at the start of the reaction? b. What is the value of the rate constant (k) if the reaction is first order? C. What is the...
Here is a graph of the molarity of butyl chloride (C,H,CI in a reaction vessel during a certain chemical reaction. Use this graph to answer the questions in the table below. x 6 ? 0.00198 M 0.00149 0.001+ 0.0007587 0 500 1000 1200 1500 2000 2450 3000 seconds created destroyed Is C HCl being created or destroyed by the chemical reaction? neither created nor destroyed xs ? If C,H Cl is being created or destroyed, what is the rate at...
Questions 2-10 please!! 1) A substitution reaction is: [2] a) A reaction during which an OH group of a molecule is replaced by a halogen. b) A reaction during which water is the leaving group. c) A reaction during which a functional group of a molecule is replaced by an electrophile. d) A reaction during which a functional group of a molecule is replaced by another functional group. V 12 2) Substitution reactions are classified either as electrophilic or nucleophilic...
please Answer in Details showing all the steps. Thank you Look at the following reaction: Toluene OH + CH3OH OCH3 + H2O a) What is the effect of each of the given changes (see next page) on the rate of the reaction? The possible answers are: Increases, decreases, remains the same or no more reaction. 1- Decreasing the concentration of CH,OH 2-Using a Dean-Stark apparatus (used to remove water from the reaction mixture) 3- Adding H,SO, to the reaction mixture...
13 SN1: Synthesis of tert-Butyl Chloride Alkyl halides can be prepared from their corresponding alcohols via an acid catalyzed substitution reaction. The mechanism of these acid catalyzed substitution reactions are labeled as Syl (substitution, nucleophilic, unimolecular) and S2 (substitution, nucleophilic, bimolecular). Tertiary alcohols follow the Snl route, primary alcohols follow the S2 route, and secondary alcohols can follow either path. Under acidic conditions, the mechanism (Figure 1) of the Sul reaction involves rapid protonation of the alcohol, followed by the...