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Organic Chemistry Full Course Bundle – Summaries, Reaction Sheets & Exam Notes – Complete Study Guide 2025

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This complete Organic Chemistry study guide includes detailed summaries, reaction sheets, and key concept overviews for both introductory and advanced topics. It covers everything from basic bonding and structure to complex synthesis and mechanisms. Perfect for students looking for an all-in-one resource that consolidates the entire course into clear and concise notes.

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ORGANIC CHEMISTRY EXAM | APPROVED QUESTIONS AND
ANSWERS | GRADED A+ | LATEST 2025-2026


A large excess of both H2O2 and I- means that the rate equation is
simplified to rate=k(H+)

Explain why the use of a large XS of H2O2 and I- means that the rate
of reaction at a fixed temperature depends only on
the concentration of H+ ions (2) - Correct Answer✔✔-- there are
negligible changes on rate as h2o2 and I- concentrations are constant
- H2O2 and I- are in zero order

An additional step is required in proton NMR for the identification of
NH3 and OH- groups

Describe this additional step and explain why it is necessary [2] -
Correct Answer✔✔-- D20 is added and mixed with the sample
- deuterium replaces the hydrogen on the OH and NH so peaks for
those do not show in the second spectrum making them identifiable

Describe how you would carry out a simple test tube reaction to
confirm that the sample of propanal obtained by distillation does not
contain any propanoic acid (2) - Correct Answer✔✔-add sodium
carbonate
effervescence - propanoic acid is present

Describe how you would distinguish between separate samples of
the two enantiomers of the branched aldehyde C5H10O - Correct
Answer✔✔-- shine plane polarised light
- each enantiomer will rotate in opposite directions

Explain how the oxides of nitrogen are formed in engines - Correct
Answer✔✔-reaction of nitrogen and oxygen in the air forming NO2
1

, 2

at high temperatures
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explain what is meant by the term homologous series [2] - Correct
Answer✔✔-- compounds with the same functional group
- each successive member differs by CH2

Explain why amine U is a weaker base than amine W. (3) (U is a
aromatic amine) - Correct Answer✔✔--Lone or electron pair on N
-Delocalised or spread into ring in U
-Less available (to accept protons) or less able to donate (to H+)

explain why bond length data helped disprove the Kekule model and
was used as evidence for the delocalised model [2] - Correct
Answer✔✔-- the bond lengths in benzene are all the same
- bond length value is between the bond lengths of the kekule model
- in kekule model there would have been two values for

explain why compound K is the major product in the reaction after
electrophilic addition (3) - Correct Answer✔✔-- K is formed from a
more stable carbocation
- major product is formed from from tertiary carbocation
- stability is sue to more electron releasing alkyl groups than a
secondary carbocation

explain why it is important to open the tap of the separating funnel
periodicaally - Correct Answer✔✔-to avoid pressure build up and
release pressure

Explain why NaBH4 reduces 2-methylbutanal but has no reaction
with 2-methylbut-1-ene. - Correct Answer✔✔-H- ion is attracted to
the s+ on THE CARBOPN ATOM
C=C in 2-methylbut-1-ene is electron rich
so H- nucleophile is repelled

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