1) Write the reaction for when 2-methyl-1-pentene reacts with HCl. Give the IUPAC name of the product formed and identify the reaction as addition or substitution type.
2) Write the reaction for when benzene reacts with Cl2 in the presence of an iron catalyst (single chlorinations). Identify the reaction as addition or substitution type.
3) Write the reaction for when pentane reacts with Cl2 under UV light (single chlorinations). Give the IUPAC name of the product formed and identify the reaction as addition or substitution type.
1) Write the reaction for when 2-methyl-1-pentene reacts with HCl. Give the IUPAC name of the...
give the name of the major product formed shen HCl reacts with
2-pentene
Give the name of the major product formed when HCl reacts with 2-pentene. O 3-chloropentane O 2,3-dichloropentane O 24hloropentane O There are no major or minor products. There is a 50/50 mixture of both O The reaction doesn't occur.
What is made when 4-methyl-2-pentene reacts with HCl?
3. Give the structures of the two products for addition reaction of HCl to 3-methyl-1-pentene (1 point). Point out which one is the major product, and explain why! (Hint: don t forget carbocation rearrangement)
Question 11 Give the IUPAC name of the compound formed when methylamine reacts with 2- pentanol in the presence of aluminum oxide and elevated temperatures. Careful with spelling enter your answer here
Write the reaction of hydration of 2-methyl-1-butene. What is the IUPAC name of the reaction product? What is the IUPAC name for the compound below? Write the dehydration reaction of this compound. What is the name of the major product? CH3 OH || CH3 - CH - CH – CH3
Bonus 3. Give the structures of the two products for addition reaction of HCl to 3-methyl-1-pentene (1 point). Point out which one is the major product, and explain why! (Hint: dont forget carbocation rearrangement) 4. The transformation of the alkyl chloride shown below into the alcohol can be accomplished in two steps. Show the synthetic scheme to finish the conversion. (1 point) Он Br
4-chloro-2-methyl-2-pentene reacts with acetic acid (solvent), two substitution products are urmea, with the rearranged product predominating as shown in the diagram that follows. When small amounts of acetate ion are added to the reaction mixture, no increase in the rate is observed. Propose a mechanism that accounts for these results. Explain clearly why two products are formed (5 points) Minor Major
In an addition reaction to an alkene, the pi bond plays the role of nucleophile electrophile leaving group Select the product that results from the anti-Markovnikov/syn addition of H and OH to the following alkene. I II III IV What is the IUPAC name for the molecule shown below? 3-(l-butynyl)pentane 5-ethyl-3-octyne 3-ethyl-4-heptyne 5-ethyl-3-heptyne What would be the major product obtained from the addition of HBr to 2-methylpentene? 1-bromo-2-methylpentane 2-bromo-2-methylpentane 3-bromo-2-methylpentane 1-bromo-2-methylpentene What is the reaction product when 4-methyl-2-pentyne is reacted...
give the IUPAC name for molecule formed from a cross condensation reaction between cyclopentanone and methyl formate
Answer them accordingly thank
you!
Question 1 a) Give the mechanism for the reaction below: 3-ethyl-3-methyl-1-pentene + HBF3-bromo-3-ethyl-2-methylpentane b) The questions are based on the reaction scheme as shown below: H202 BH3 NaOH, H20 i) Determine the structure of intermediate A and product B. ii) The formation of product B follow one rule in electrophilic addition. What is the name of the rule and explain that rule. i) Give one reagent that can be used to reduce the alkyne above...