please help me with the question below: Consider Table 4 and suggest why BrCH2CH2Br (35.8 vs. 5.7) has a higher SN2 reaction rate than FCH2CH2Br.
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please help me with the question below:
Consider Table 4 and suggest why BrCH2CH2Br (35.8 vs. 5.7) has a higher SN2 reaction rate than FCH2CH2Br.
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- Predict the products by showing the reaction mechanism (arrow pushing) of the given diagram.1. MCPBA; H3O+ 2. OsO4, Na2SO3/H2O 3. H3O+Which of the following correctly completes the reaction? C5H12 + O2 → ? C5H12 + 302 → 5C + 6H2O O C5H12 + 8O2 → 5CO2 + 6H2O C5H12 + 502 → 5CO2 + 6H2 C5H12 + O2 → C5H1202Which of the following represents the transition state of the rate- determining step in the reaction between 2-bromopropane and sodium methoxide leading to elimination? H;C H;C CH, S0----H----CH2 CH3 -Br -Br 2 H3C CH, Br H3C CH: ---Br 3 H3C а. 1 b. 2 с. 3 d. 4
- Which mechanism is consistent with the reaction below?2NO+2H2→N2+2H2O 1. NO+H2→NOH22. NOH2+NO→N2O2+H23. H2+ N2O2→ N2+H2O 1. NO+H2→N+H2O2. NO+H2→N+H2O 1. NO+H2O→NO2+H22. NO2+H2→N2+H2O 1. 2NO⇄N2O22. N2O2+H2→N2O+H2O3. N2O+H2→N2+H2OHow many transition states and intermediates would the reaction profile have for the reaction shown below?Below is the equation for a nucleophilic substitution reaction and some experimental data. CH3CH2Br + CH3COO- ⇌ CH3CH2CO2CH3 + Br- ΔH=-75 kJ/mol Rate = k [CH3CH2Br][CH3COO-] Which reaction energy profile would be the best representative of the data provided?
- 17. Which of the following is a mechanism for an SN2 reaction? III. نعت a. I b. II c. III d. IV e. Both I & II LAM Br CN O + Br IV - Br + BrSECTION 6: Show the mechanism of each reactions with arrows and intermediates form as in a. b. C. HBr Br₂ Cl₂, H₂O Br Br CI Br OH6. Complete reaction scheme below indicating reagents, catalysts and conditions, and side product trigil bezinslog si6101fon 290b 1l (b Senines levirba 6 gaubong nasamots gniwollot ads to doinW 01 sniowl (6 CH3 40 CH3 Scansgowi (d Ege nodie) ( nsgyxo (b NO₂ 19m02 2i gniwollet sits to mainW II HO
- The following is a nucleophilic substitution reaction of S-3-chloro-2-methylhexane with "CN. The experimental rate law for this reaction is Rate k [S-3-chloro-2-methylhexane] CH3 H;C. C. C H. CH3 CEN H2 H. The mechanism for this reaction is SN1 Draw the orgamic molecule(s) which is(are) formed in this reaction. Do not include molecules like H,O or HCl. Draw the specific configuration (R or S) at any chiral carbons within your product(s). If both configurations are formed in the product(s), draw both as separate molecules/products.Which of the following parameters affects the rate and kinetics of a reaction? A. Solvent medium B. Reaction temperature C. Reaction time D. Geometry and structure of the alkyl halide E. pH4. Outline a detailed mechanism for the reaction below. Identify the abbreviation for the reaction mechanism. НО H3PO4