subject
Chemistry, 11.12.2019 21:31 timjape3g3z

Compound w, c6h11cl, undergoes base-promoted e2 elimination to form a single alkene y. under similar reaction conditions x, c6h11br, affords y and an isomeric alkene. catalytic hydrogenation of y produces methylcyclopentane. w readily undergoes an sn2 reaction with sodium iodide in acetone. x does not undergo a similar sn2 reaction. what are the structures of w and x?

ansver
Answers: 2

Another question on Chemistry

question
Chemistry, 22.06.2019 02:30
What does the cell nucleus do or, how does it function?
Answers: 1
question
Chemistry, 22.06.2019 20:00
For the reaction c6h14(g) & longrightarrow; c6h6(g) + 4h2(g), δp(h2)/δt was found to be 2.5 x 10-2 atm/s, where δp(h2) is the change in pressure of hydrogen. determine δp(c6h14)/δt for this reaction at the same time.
Answers: 2
question
Chemistry, 22.06.2019 22:30
Write and balance the chemical equation that represents the reaction of aqueous sulfuric acid with aqueous sodium hydroxide to form water and sodium sulfate. include phases.
Answers: 1
question
Chemistry, 23.06.2019 00:00
2-bromo-2-methylbutane undergoes an e1 elimination reaction in the presence of ethanol. in the next reaction only one of the possible products is represented. although the product shown is not the major product of the reaction, notice that there is more than one way it can be produced. complete the mechanism and draw the missing substances.
Answers: 1
You know the right answer?
Compound w, c6h11cl, undergoes base-promoted e2 elimination to form a single alkene y. under similar...
Questions
question
Physics, 02.03.2020 22:38
Questions on the website: 13722363