ANS-Monomers 1 and 2 both have hydrogen (H) and hydroxyl groups
(OH) attached to them. When they come together with an appropriate
catalyst (an atom or a molecule that speeds up the chemical
reaction without being used up in it), one monomer loses a hydrogen
while the other loses a hydroxyl group. The hydrogen and hydroxyl
groups combine to form water (H2O), and the remaining electrons
form a covalent chemical bond between the monomers. The resulting
compound is the basic subunit of copolymers 1 and 2. This reaction
occurs over and over again until you get a long chain of copolymers
1 and 2.THANK
YOU VERY MUCH.
Show condensation reaction between an alcohol group from one monomer with an alcohol group from the...
Show condensation reaction of acetophenone. Show condensation reaction of propanal with benzaldehyde. Show condensation reaction of ethyl acetate. Mechanisms would be great!
a) Show the Aldo condensation reaction between cyclohexanone and 4-methoxybenzaldehyde with a base catalyst. Show all steps. b) Write a balanced reaction equation of this Aldo condensation
* Discussion Questions, continued. Kodel"is a condensation polymer produced by the co-polymerization of the two monomer molecules shown below Draw the 1,4-dihydroxymethyleyclohexane and rwo of terephthalic acid, in alternating order). Identify the two reactant functional groups, and the functional group of the linkage that's formed. When the polymer forms, thousands of these molecules link together (in alternating order) via condensation reactions. structure of a portion of a "Kodel"molecule by linking together FOUR of the reactant molecules (nwvo of он н...
Esters are formed by condensation reaction (removal of H2O molecules) between a carboxylic acid and an alcohol where the acid loses a proton (H+) and the alcohol loses a hydroxide anion (OH-) a. True b. False
a)
show the reaction mechanism for this condensation reaction
b) of all the possible products there is one dominant, which
one and why? And what will work as a nucleophile?
Bas
a) Draw all of the products obtained from the base-catalyzed aldol condensation reaction between butanal and pentanal(crossed and self) b) Show the half reaction corresponding to the reduction of permanganate ion to manganese dioxide. Show the half reaction corresponding to the oxidation of cyclopentene to 1,2 dihydroxycyclopentane. Add the two half-reactions together to give the overall net ionic equation of the oxidation of cyclopentene to 1,2 dihydroxycyclopentane using permanganate ion. Can anyone help me out?
The Claisen condensation converts 2 molecules of an ester into a
?-keto ester. The reaction starts with the ester in an
alkoxide/alcohol solution and is worked up with acid to form the
neutral ?-keto ester product.
Please show what goes in each box!! What I put shown below are
all incorrect.
The Claisen condensation converts 2 molecules of an ester into a β-keto ester. The reaction starts with the ester in an alkoxide/alcohol solution and is worked up with acid...
Show the product after the addition of 6 monomer in the
following reaction
RO OR + H
give the IUPAC name for molecule formed from a cross condensation reaction between cyclopentanone and methyl formate
Provide the detailed mechanism of the aldol condensation reaction between 2 mols of benzaldehyde and 1 mol of acetone under basic conditions. Show all intermediates and steps for full credit. There are 10 steps to the complete mechanism. Please help me with this one.