ANSWER:-
limiting reactant is that reactant in which less number of moles are involved.
so for calculation number of moles we use the formula n=w/m
so for 4-tert-butylcyclohexanone w = 0.498 g
molar mass of 4-tert-butylcyclohexanone 154.25 g/mol
so number of moles = 0.498/154.25
n = 0.003229 moles that is 3.22 mmol of 4-tert-butylcyclohexanone
number of moles for m-chloroperoxybenzoic acid = w/m
mass of m-chloroperoxybenzoic acid 172.57 g/mol
n = 1.132 / 172.57 = 0.00656 moles that is 6.56 mmol of m-chloroperoxybenzoic acid
so here limiting reactant is 4-tert-butylcyclohexanone because of less moles (3.22)
now determination of molar equivalents for determine the molar equivalents we should know the limiting reactant and their moles so here we know that limiting reactant is 4-tert-butylcyclohexanone (3.22 mmol).
calculate molar equivalents for each reagent, divide the moles of that reagent by the moles of the limiting reagent
molar equivalents for 4-tert-butylcyclohexanone = 3.22/3.22 = 1 equivalent
molar equivalents for m-chloroperoxybenzoic acid = 6.56mmol/3.22mmol = 2.04 equivalents.
in a solvent free Baeyer-Villiger reaction, the mass of the starting material or 4-tert-butylcyclohexanone is 0.498g,...
7. (5 points extra credit) Baeyer-Villiger Oxidation! When tert-butyl methyl ketone is reacted with mCPBA and base, the ketone is cleanly converted to a single ester product in high yield (A or B). Circle the product of this reaction (A or B) and explain your answer (explain the migratory ability of t-Bu vs Me).
The Baeyer-Villiger reaction is classified as an “oxidation” reaction. What is the chemical species that's being oxidized in this reaction? What is the chemical species that is being reduced?_ Baeyer-Villiger Reaction of Acetophenone Data Results • Moles of acetophenone used: (Show calculations) 0.020 moles (2.40g/120.151 g mol-1 =0.0199 moles) • Moles of mCPBA used: (Show calculations) 0.036 moles_(6.25 grams/ 172.56 g.mol-1) • Expected mass of the product: (Show calculation. Clearly show the limiting and excess reactants)
sodium borohydide reduction of 4 tert
butylcyclohexanone. need help confirming top answers are correct
and help with lower section. thanks
& Draw your two products (each in the most stable chair conformation) below using the numbering provided. Show only the -OH and tert-butyl groups on the ring. a) label each group as equatorial (eq) or axial (ax). b) label each group as top face (top) or bottom face (bot). OH (ax, top) (ax, bot) .OH (Eq, top 7 (Er, top...
Baeyer Villiger
Can someone explain the GCMS of this sample?
This was the procedure:
A solution of acetophenone, 20 mmoles, and
metha-chloroperbenzoic acid (mCPBA)
36mmoles, are stirred in 50mL of distilled water at 80°C for 4 h
and monitored by
TLC (eluent: ethyl acetate). The reaction mixture is cooled to
room temperature and
extracted with dichloromethane (3x30mL). The combined organic
layers are
washed with saturated NaHCO3, and NaCl brine solution. The
solution is then dried
with MgSO4 and the solvent...
Compound B, tert-butanol, is a polar, protic molecule that can
be used as a solvent for E1 reactions. True or False. Explain.
2. True or False Compound B, tert-butanol, is a polar, protic molecule that can be used as a solvent for E1 reactions. used for Ez H ou HC CH3 3. True or False Chloromethane and sodium acetate react to produce methyl acetate by an Sn1 mechanism. OH H + NaCl H HCONa OH CI H I fastest slower...
just the balanced equations for main reaction and side
reaction with steps and major / minor products please and thank
you
can you create a balanced stereoselective mechanism
equation for both reactions using the 4tertbutyl starting base
equation from the 1st previous image for the primary reactions and
side reaction equations on the 2nd previous image. and can you also
include any major and minor products please and thank you
STEREOSELECTIVE REDUCTION OF 4-tert-BUTYLCYCLOHEXANONE OH 1. NaBH4, EtOH 2. H30+...
13 SN1: Synthesis of tert-Butyl Chloride Alkyl halides can be prepared from their corresponding alcohols via an acid catalyzed substitution reaction. The mechanism of these acid catalyzed substitution reactions are labeled as Syl (substitution, nucleophilic, unimolecular) and S2 (substitution, nucleophilic, bimolecular). Tertiary alcohols follow the Snl route, primary alcohols follow the S2 route, and secondary alcohols can follow either path. Under acidic conditions, the mechanism (Figure 1) of the Sul reaction involves rapid protonation of the alcohol, followed by the...
i
need help with this
Mass of sodium bromide used = 11.09 Volume of butyl alcohol used = 10.0 ml 1a. Mass of butyl alcohol used (calculate; show work) = Mass of the pre-weighed E-flask or beaker =..... Mass of pre-weighed E-flask or beaker + crude product (n-butyl bromide) = 102.6-98.8 ....101.609... 1 b. Mass of the crude product (n-butyl bromide - show work) =................... Ic. Theoretical yield based on each of the starting materials (Please use two Dimensional Analysis...
This is a Solvent-Free Synthesis of Chalcones: Claisen-Schmidt
Condensation
The Chalcone starting materials are:
p-bromoscetophenone (solid)
p-chlorobenzaldehyde (solid)
6. [1pt] When you treated the reaction TLC with 2,4-dinitrophenylhydrazine solution, you must have observed that the starting materials show up as bright orange spots instantaneously, whereas the product either shows no change or appears as a faint spot. Explain this observation. 8. [1 pt] 4-chlorobenzaldehyde and 4-bromoacetophenone are both solid starting materials for the synthesis of substituted chalcone. When both of...
13 SN1: Synthesis of tert-Butyl Chloride Alkyl halides can be prepared from their corresponding alcohols via an acid catalyzed substitution reaction. The mechanism of these acid catalyzed substitution reactions are labeled as Syl (substitution, nucleophilic, unimolecular) and S2 (substitution, nucleophilic, bimolecular). Tertiary alcohols follow the Snl route, primary alcohols follow the S2 route, and secondary alcohols can follow either path. Under acidic conditions, the mechanism (Figure 1) of the Sul reaction involves rapid protonation of the alcohol, followed by the...