Tertiary alkyl halides undergo SN1 reaction to form newly substituted product as tertiary carbocations are more stable than secondary and primary
Tertiary alkyl halides undergo E1 reactions in presence of water or alcohol. If you use strong bases like OH¯ or RO¯, it will undergo E2 reaction
Now the given reaction undergo SN1 reaction and E1 reaction
B product forms by SN1 and E product formed by E1
26) Alkenes undergo epoxidation in presence of mCPBA. In this reaction the stereochemistry will be retained as per the starting material. Cis alkene upon reaction with mCPBA gives cis product and trans alkene gives trans product.
Select the mechanism(s) that would occur in this reaction and select all the possible products, you...
One of the possible answers may be "no reaction".
Thank you in advance
Practice Question 34 Give the major product of the following reaction. H2 Ni Practice Question 35 Give the major product of the following reaction. H2 Lindlar's Catalyst Practice Question 36 Give the major product of the following reaction. NH3 (liq) Practice Question 37 Give the major product of the following reaction. Na NH3 (liq). Practice Question 38 Give the major product of the following reaction. We were...
Which isotope is not possible?
Select one:
a.
b.
c.
d.
e. All of these isotopes are possible.
We were unable to transcribe this imageWe were unable to transcribe this image[OH] [H3O] [OH]
QUESTION 1 Select all products formed. Wrong answers count against you. H/Pd יווווווווון We were unable to transcribe this imageQuestion 1 Cl2/CC14 ・・ 」 MIL TIT O . milla JIII
for possible organic products from the following reaction via
sn1 and sn2 mechanism select the one with the lowest heat of
combustion
QUESTION 11 11) For possible organic products from the following reaction via Sul or S 2 mechanism (both a possible): select the one with LOWEST Heat of Combustion: or organic + CH2OH → product + HBr D. CHO* -- or to werden med barn when we OCH3 .CH OH CH3 H2C are
Please help!!!!! The mechanism would be nice too
For the reaction below provide all possible product(s), hand draw the products on a piece of paper and circle the major product. No cutting and pasting from the Internet, You can only upload an image of your response, Initial your name next to each response. Br Ph3P Butyl Lithium 2 Butanone ether ether Br
Problem 7.28 Propose a mechanism for the following reaction DCI Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with bonds. Add charges wher should start on the electron(s) of an atom or a bond and should end on an atom, bond, or location where a new bond should be created. Use water to rep isotopic form of hydrogen, right-click the atom and choose Atom Properties (Mac users: Use an...
Consider the following reaction NaOEt ------>EtOH a) Identify the mechanism(s) by which the reaction will occur. If there is more than one mechanism that can operate, identify the mechanism that will predominate. Explain your reasoning clearly. b) Predict all possible product(s) that will be formed and identify them as major and minor products.
Let
Which of the following are TRUE? Select ALL that apply. Please
show all your work.
a.
has a local maximum at
whenever
is an even integer
b.
has a saddle point at
whenever
is an even integer
c.
has a saddle point at
whenever
is an odd integer
d.
has a local minimum at
whenever
is an odd integer
fr, y) = sin(x + 7/2) +y? We were unable to transcribe this imageWe were unable to transcribe this imageWe...
How many distinct derivations of bcde are possible using
S BCDE
B b
C c
D d
E e
We were unable to transcribe this imageWe were unable to transcribe this imageWe were unable to transcribe this imageWe were unable to transcribe this imageWe were unable to transcribe this image
Which of the following rings are Unique Factorization Domains?
Select all that apply.
We were unable to transcribe this imageQC We were unable to transcribe this imageWe were unable to transcribe this imageWe were unable to transcribe this imageWe were unable to transcribe this image