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Recent activity in Organic Chemistry
0
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1
answer
29
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How can Spectroscopic techniques be used to identify the functional groups present in an organic compound? Provide an example of how this technique can be used to determine the functional groups in a given compound.
answered
6 hours
ago
in
Organic Chemistry
by
MattSchaefer
(
710
points)
0
votes
1
answer
32
views
How can a chemist selectively protect an amine group in the presence of hydroxyl and carboxyl groups when synthesizing a complex organic molecule using protecting groups?
answered
23 hours
ago
in
Organic Chemistry
by
Eli39B708868
(
450
points)
0
votes
1
answer
35
views
How can 1-bromo-2-methylcyclohexane be transformed into 1-methylcyclohexene via an E2 elimination reaction? What are the necessary conditions and reagents needed for this transformation to occur?
answered
23 hours
ago
in
Organic Chemistry
by
StefanieDadd
(
610
points)
0
votes
1
answer
19
views
Here's a precise problem for the student to solve:What is the oxidation state of carbon in ethanol (C2H5OH)? Show the electron transfer steps involved in the oxidation of ethanol to acetic acid (CH3COOH) using balanced half-reactions.
answered
23 hours
ago
in
Organic Chemistry
by
NikiCoombs07
(
590
points)
0
votes
1
answer
31
views
Here's a precise problem for a chemistry student to solve in Organic Synthesis and Retrosynthesis:Develop a retrosynthesis approach to synthesize 2-methyl-1-phenylpropan-1-ol, starting from benzene, propene, and any other necessary reagents, explaining each step in the backward reaction sequence.
answered
23 hours
ago
in
Organic Chemistry
by
MatthewPuig
(
570
points)
0
votes
1
answer
20
views
Here's a precise problem for a chemistry student to solve based on the subtopic Rearrangement reactions:What products form from the acid-catalyzed rearrangement of 2-methyl-3-butene to form 3-methyl-1-butene? Use mechanisms to explain why this rearrangement occurs.
answered
23 hours
ago
in
Organic Chemistry
by
EssieHimes15
(
350
points)
0
votes
1
answer
5
views
Design a synthetic route to prepare (Z)-4-octene from 1-octyne using any suitable reagents and reaction conditions, while achieving a high yield and selectivity for the desired (Z)-isomer.
answered
1 day
ago
in
Organic Chemistry
by
Rhea03G2525
(
410
points)
0
votes
1
answer
30
views
Design a synthesis route for the heterocyclic compound Pyridine starting from benzene as the starting material, using the commonly used reactions in organic chemistry and displaying the steps involved in the reactivity of each reaction.
answered
1 day
ago
in
Organic Chemistry
by
KathrinDesco
(
370
points)
0
votes
1
answer
26
views
Design a synthesis pathway for the production of 2-butyne from 1-bromobutane, including all necessary reagents and reaction mechanisms.
answered
1 day
ago
in
Organic Chemistry
by
JeffrySchuhm
(
390
points)
0
votes
1
answer
20
views
Design a strategy to protect the alcohol functional group in a molecule containing both a primary amine and a carboxylic acid group, to prevent unwanted reactions during organic synthesis.
answered
1 day
ago
in
Organic Chemistry
by
PauletteAmie
(
530
points)
0
votes
1
answer
38
views
Design a retrosynthetic pathway to synthesize ibuprofen starting from methylcyclohexane. Show all necessary reagents and the key steps involved in the synthesis.
answered
1 day
ago
in
Organic Chemistry
by
PearlineNewe
(
450
points)
0
votes
1
answer
5
views
Design a retrosynthesis plan to synthesize ibuprofen from benzene.
answered
1 day
ago
in
Organic Chemistry
by
IlaScorfield
(
550
points)
0
votes
1
answer
22
views
Design a retrosynthesis pathway to synthesize benzyl alcohol from benzaldehyde using the appropriate reagents and reaction conditions.
answered
1 day
ago
in
Organic Chemistry
by
BKDMyra3361
(
490
points)
0
votes
1
answer
6
views
Design a retrosynthesis pathway for the synthesis of ibuprofen from starting materials that have no more than 6 carbons.
answered
1 day
ago
in
Organic Chemistry
by
EarnestDesco
(
550
points)
0
votes
1
answer
19
views
Design a retrosynthesis for the synthesis of the following compound: 2-ethyl-3-methylcyclopent-2-enone using the Grignard reaction as the key step. Show all the necessary reagents and reaction conditions.
answered
1 day
ago
in
Organic Chemistry
by
CamillaTyner
(
470
points)
0
votes
1
answer
4
views
Design a retrosynthesis for the synthesis of 2-phenylpropionic acid from benzene, ethylene, and CO₂.
answered
1 day
ago
in
Organic Chemistry
by
Mose92K00958
(
330
points)
0
votes
1
answer
30
views
Design a polymerization reaction to produce a high-density polyethylene (HDPE) with a molecular weight of 1 million grams per mole using ethylene as the monomer and a Ziegler-Natta catalyst system. Calculate the theoretical yield of the reaction and explain the factors that may affect the percent yield.
answered
1 day
ago
in
Organic Chemistry
by
GonzaloBecer
(
530
points)
0
votes
1
answer
33
views
Design a polymerization reaction scheme to synthesize a biodegradable and water-soluble polymer for use in environmentally friendly packaging materials.
answered
1 day
ago
in
Organic Chemistry
by
AdaBrigstock
(
370
points)
0
votes
1
answer
29
views
Design a multi-step synthesis of 2-phenylbutanoic acid starting from benzene and any other necessary reagents, using retrosynthesis to plan the reaction steps. Include reaction mechanisms, reagents, and conditions for each step.
answered
1 day
ago
in
Organic Chemistry
by
GaryLepage93
(
290
points)
0
votes
1
answer
19
views
Design a heterocyclic compound using pyridine as a starting material and incorporating at least one nitrogen atom in the heterocyclic ring. Draw the reaction mechanism involved in the synthesis and explain the role of each reagent used in the synthesis.
answered
1 day
ago
in
Organic Chemistry
by
LolaSilas675
(
370
points)
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Recent activity in Organic Chemistry
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