What compound results is the 1,2-addition product of the reaction below: 1 mol HBr 1-bromo-1-butene 2-bromo-2-butene 4-bromo-1-butene 3-bromo-1-butene 1-bromo-2-butene O O
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- I got confused with the steps provided. In m= it should have an exponent raised to (-10) but during Step 2, the exponent (-10) in m is omitted. Second, I do not know the basis of the formula used in Step 2. Please provide a better explanation of the solution. Thank you.Choose the best reagents from the list provided below for carrying out the following conversion. Match the reagent with the step number. HCl (aq), Zn(Hg) KMnO4, H3O+ CH3Cl, AlCl3 HNO3, H2SO4 Cl2, FeCl3 fuming sulfuric acidConsider the series of the trans effect: CO, CN-, C2H4 > PR3, H-, CH3- > C6H5- > NO2-, SCN-, I- > Br- >Cl- > py > NH3 > H20 What would be the major product of the following reaction? Select one:
- Draw the major 1,2- and 1,4- addition products formed when this diene reacts with HCl. Do not include any byproducts. Show your work.What substrates are needed to synthesize the conjugate addition product below? a) 1 and 3 b) 2 and 3 c) 1 and 4 d) 2 and 4Starting materials: 1.80g metals/magnesium 5.65mL Bromopropane 3.04mL 4-methoxybenzaldehyde (limiting reagent) Product (1-(4-methoxyphenyl)-methyl propan-1-ol) 3.40g How to Calculate the percent yield of the Product (1-(4-methoxyphenyl)-methyl propan-1-ol). Show works and details please
- Hello, could not figure out the steps i should follow, and which one to use from the fiven information.Can you help me label this irBelow, t-butyl chloride (molecular ion = 92) has been marked for "splitting" in MS, just as in the lecture. Find the correct values for A, B, C, and D. NOTE: B and D have more than one correct value because of something in the molecule!
- Help ASAP Illustrate the resonance effect of the methoxy group -OCH3, on the structure of the benzene ring. Do this by writing all the possible resonance forms for methoxybenzene, including the hybrid. Based on your structures, explain how the presence of the -OCH3 group affects: (i) the reactivity of the benzene ring towards electrophilic attack; (ii) the orientation or point of attack of an incoming electrophilic reagent on the benzene ring.1.) Predict the reactivity of the following alkyl bromides in a substitution reaction with NaI in acetone. Rank them from 1-2 with 1 being the fastest and circle the molecule(s) that reacted in the substitution experiment? 2.) Rank the molecules from 1-2 based on their rate of reactivity with NaI with 1 being the fastest. Explain the theory behind your ranking of each compoundthanks. only b-d.