In radical reactions, there are sometimes non-halogenated side products formed from other termination steps. Choose the possible side product of the reaction shown below? = Br2 hv IV A | B C = III = D IV
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- Is this correct?In radical reactions, there are sometimes non-halogenated side products formed from other termination steps. Choose a possible side product of the reaction shown below? I, II, III, IV?The propene reaction with OH radical has a reaction rate constant 2.63 * 10-11 cm3/(molecules*s) and the reaction rate constant with O3 is 1.13*10-17 cm3/(molecules*s). Under polluted conditions (OH=1*106 molecules/cm3 and O3=125 ppb), which reaction dominates? (Assume T=30°C)
- 4. Explain why the rate of formation of 1-azidopropane is different depending on which halopropane (X = F, Cl, Br, I) is used. Explain which halopropane will react fastest? ~X X = F, Cl, Br, I NaN №3 1-azidopropaneFf.268.What is the kinetically controlled product in the following reaction? A Br OA. A OB. B О с. с OD. D B Br HBr ?? C Br Br D
- C5H8 + 7O2 → 5CO2 + 4H2O type of reactiong) A series of reduction experiments was carried out at a given temperature. The results are summarized in Table 2 below. Determine the rate law expression for this reaction. [ 12 Table 2-Experimental rate measurements [R] (mol L³) [Methan-1-ol] (mol L¹) Rate (mol L¹s¹) 0.100 0.100 2.40 x 10² 0.100 0.300 7.20x10² 0.300 0.100 2.16 x 10¹ h) Below are two proposed reaction mechanisms for this reaction. Explain which reaction mechanism is correct. [ (Let Box methan-1-ol; BA= methanal; B = methanoic acid, R = reducing agent) Mechanism 1 Mechanism 2 BH+R BA (slow) BH+R BA (fast) BA+RBOH (fast) BA+R BON (slow)Fill in the missing information—reactants, intermediatesor products—in each of the following reactions. One of these reactions does not take place as written—if no reaction occurs, state “NR”.
- The following is a nucleophilic substitution reaction of R-3-bromohexane with "SH. The experimental rate law for this reaction is Rate = k [R-3-bromohexane] [SH] H. H.C C. CH3 SH H2 Br H. The mechanism for this reaction is SN2 Draw the organic 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.CH,CH,СH, CI CH,СНHCICH, + 2HCI 2CH,CH,СH, + 2C1, The chlorination of propane proceeds as a radical chain reaction. Sort the 7 reaction steps (you may need to scroll down to see them all) into categories of: Initiation Propagation Termination сн, сH,CH,. CH3CH2CH2 CH,CH, CH, -di: сHсHCH- di: а — б: — 2б Cl CH3CH2CH2 CнснсH. СH,сH,CH, -н CH3CHCH3 н— н—й: сн,бнсн, CH,CнсH, CH CHCH сH,снсH,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.

