Question
In: Chemistry
Choose all possible reagents for the reaction of a primary alcohol to alkyl halide and, for...
Choose all possible reagents for the reaction of a primary alcohol to alkyl halide and, for part B, choose all possible reagents for a primary alcohol to alkene reaction A) HBr with heat, thionyl chloride with base, HCl with heat, PBr3, concentrated sulfuric acid with heat, HF with heat, NaOH with heat B)concentrated sulfuric acid with heat, HCl with heat, HF with heat, NaOH with heat, PBr3, thionyl chloride with base, HBr with heat
Solutions
queen_honey_blossom answered 2 years agoRelated Solutions
Part A Draw the alcohol and the alkyl halide that would be used to synthesize cyclohexyl...
Part A Draw the alcohol and the alkyl halide that would be used
to synthesize cyclohexyl propyl ether by Williamson ether
synthesis.
Draw the molecules on the canvas by choosing buttons from the
Tools (for bonds and charges), Atoms, and Templates toolbars.
Part B
Draw the alcohol and the alkyl halide that would be used to
synthesize isopropyl methyl ether by Williamson ether
synthesis.
Part C
Draw the alcohol and the alkyl halide that would be used to
synthesize 1-methoxy-4-nitrobenzene...
Name the possible products of an oxidation of a primary alcohol. Include appropriate oxidizing reagents for...
Name the possible products of an oxidation of a primary alcohol.
Include appropriate oxidizing reagents for these products.
How many of the following responses are true? 1. A primary alkyl halide will tend to...
How many of the following responses are true?
1. A primary alkyl halide will tend to react through an SN2
mechanism because there is little hindrance to backside attack and
a primary carbocation is not very stable
2. 3-bromo-3-methylpentane will undergo substitution through an SN2
mechanism
3. If R-2-bromopentane is allowed to react with OH- the product
will be S-2-pentanol
4. SN1 leads to a racemization of sterechemistry due to the
nucleophile attacking from the backside and the leaving group...
Match the correct reagents with the description of the reaction. converts an alkene into an alkyl...
Match the correct
reagents with the description of the reaction.
converts an alkene
into an alkyl bromide (non-Markovnikov)
hydrates an alkene
(Markovnikov, rearrangements possible)
converts an alkene
into an alkyl bromide (Markovnikov)
converts an alkyne
into a geminal dibromide (Markovnikov)
reduces an alkene or
alkyne to an alkane
substitutes an H for a
Br in the position of the most stable radical
reduces an alkyne to a
trans alkene
converts a terminal
alkyne to an aldehyde (non-Markovnikov)
reduces an alkyne...
The Gabriel synthesis transforms an alkyl halide into a primary amine via a two-step process.
The Gabriel synthesis transforms an alkyl halide into a primary amine via a two-step process. Follow the directions below to draw the initial mechanism and final products. Draw curved arrows to the next step. Draw the missing nonbonding electrons, charge and curved arrows. The first three steps are correct. I am unsure about how to complete the final step.
Percent yield of alkyl halide (Show all calculations for limiting reactant, theoretical yield and percent yield.)...
Percent yield of alkyl halide (Show all calculations for
limiting reactant, theoretical yield and percent yield.) Note I
have 1.746g of product obatined of pure alkyl halide Also my unkown
that i chose for this experiment was 3-methyl-1-butanol---- I
started with 18.996g---15.281g after reflux-- 14.993g after IR
spectroscopy
Percent yield of alkyl halide (Show all calculations for limiting reactant, theoretical yield and percent yield.)...
Percent yield of alkyl halide (Show all calculations for
limiting reactant, theoretical yield and percent yield.)
Given:
R-CH2OH +NaBr +H2SO4---------> R-CH2BR +H2O+ NaHSO4
- started with - unkown alcohol: 3-methyl-1-butanol (18.996 g)
started with,
-NaBr ( 10.509g) used
-H2SO4 (25 mL of 8.7M)
-My alkyl halide is 1-bromo-3- methylbutane
-H2O
-NaHSO4
Note! I ended with 1.746g of the alkyl halide is 1-bromo-3-
methylbutane
In friedel-crafts alkylation of benzene with an alkyl halide and AlCl3: 1. In terms of intermediate...
In friedel-crafts alkylation of benzene with an alkyl halide and
AlCl3:
1. In terms of intermediate and product stabilities explain why
the ortho and para isomers would be favored under kinetic
conditions and why the meta isomer would be favored under
thermodyanmic conditions?
2. What function does the nitromethane serve in the kinetic
reaction?
3. What reactants would you employ for the preparation of the
following compounds by reactions of the Friedel-crafts type?
- a. diphenylmethane
- b. 4-bromophenyl phenyl...
how the leaving group affect the behavior of the alkyl halide in mixture of NaI/ Acetone...
how the leaving group affect the behavior of the alkyl halide in
mixture of NaI/ Acetone and in mixture of AgNO3/ Ethanol?
All of the reagents in the reaction below are in aqueous form. The initial concentration of...
All of the reagents in the reaction below are in aqueous form.
The initial concentration of A is 4.5x10-4 M. The
initial concentration of B is 5.3x10-3 M. At
equilibrium, the concetration of A is 1.2 x 10-4 M. What
is the value of Keq?
A + 2B <----------> C + 3D
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