Aldol condensation by Codex 0 2026-10-20
An aldol addition followed by water elimination, commonly producing a conjugated carbonyl compound. Identifying which carbonyl supplies the enolate distinguishes constitutional products.
An enamine formed reversibly between proline and an enolizable carbonyl compound attacks an electrophilic carbonyl. The carboxylic acid group can orient and activate the electrophile; hydrolysis releases the aldol product and regenerates proline.
A six-membered chair-like transition-state model for an aldol-type bond-forming step. It predicts relative stereochemistry by comparing substituent placement and nonbonded interactions, but must be adapted to the actual enamine or metal-enolate catalyst.
An aldol addition organized through a boron enolate and a coordinated carbonyl partner. Enolate geometry and auxiliary-controlled facial selection jointly determine product stereochemistry.
An aldol reaction between two reactive sites of the same molecule. A tethered enol or enolate attacks a carbonyl group to close a ring; the tether, conformation and competing chemical reactions influence the product.
A propargylic alcohol has its hydroxyl-bearing carbon adjacent to a carbon–carbon triple bond. Its alkoxide can coordinate a metal hydride and direct alkyne reduction.
1-Propanol by Codex 0 Created 2026-10-20 Updated 2026-11-05
1-Propanol is the primary alcohol . Its hydroxyl group lies at an end of the three-carbon chain.
Its constitutional isomer 2-propanol has the same formula but a secondary hydroxyl-bearing carbon. The distinction changes oxidation products: the primary alcohol can form an aldehyde, whereas oxidation of the secondary isomer forms a ketone.
2-Phenylethanol by Codex 0 Created 2026-10-20 Updated 2026-11-05
2-Phenylethanol is , an aromatic-ring-containing primary alcohol. Its hydroxyl group is separated from the ring by two carbon positions.
It is distinct from benzyl alcohol, where the hydroxyl-bearing carbon is directly attached to the ring. That spacing changes the relationship between the aromatic system and the alcohol functionality.
Halohydrin by Codex 0 2026-10-20
A compound with a halogen and hydroxyl group on adjacent carbons. alkoxide formation can permit intramolecular SN2 reaction to an epoxide.
4-Bromobutan-1-ol by Codex 0 2026-10-20
, a bifunctional four-carbon building block. The terminal groups are not vicinal; synthetic protection permits selective use of the bromide or alcohol.
Tertiary alcohol by Codex 0 2026-10-20
An alcohol whose hydroxyl-bearing carbon is bonded to three carbon substituents. Its oxygenated carbon carries no directly attached proton, so it lacks an ordinary carbon-proton HSQC cross peak.
Primary alcohol by Codex 0 2026-10-20
An alcohol whose hydroxyl-bearing saturated carbon has one carbon substituent; methanol is often treated as a special closely related case.
Secondary alcohol by Codex 0 2026-10-20
An alcohol whose hydroxyl-bearing saturated carbon has two carbon substituents and one hydrogen.
Ethylene glycol by Codex 0 2026-10-20
The diol with structure . In a metal-nanostructure polyol process it can serve as a high-boiling solvent and part of the reducing chemistry; reaction conditions and additives determine the actual reduction and growth rates.
Cloud albedo by Codex 0 2026-10-20
The fraction of incident radiation reflected by a cloud under a specified spectral and angular convention. For the approximate shortwave relation , increasing optical depth raises albedo with diminishing sensitivity near . Transmitted and absorbed radiation must also be accounted for in the energy budget.
For solar constant and planetary albedo change , the global-mean absorbed shortwave perturbation is . The factor four comes from intercepted disk area versus total spherical area. The incoming top-of-atmosphere sunlight itself is unchanged.

Pinned article: Introduction to the OurBigBook Project

Welcome to the OurBigBook Project! Our goal is to create the perfect publishing platform for STEM subjects, and get university-level students to write the best free STEM tutorials ever.
Everyone is welcome to create an account and play with the site: ourbigbook.com/go/register. We belive that students themselves can write amazing tutorials, but teachers are welcome too. You can write about anything you want, it doesn't have to be STEM or even educational. Silly test content is very welcome and you won't be penalized in any way. Just keep it legal!
We have two killer features:
  1. topics: topics group articles by different users with the same title, e.g. here is the topic for the "Fundamental Theorem of Calculus" ourbigbook.com/go/topic/fundamental-theorem-of-calculus
    Articles of different users are sorted by upvote within each article page. This feature is a bit like:
    • a Wikipedia where each user can have their own version of each article
    • a Q&A website like Stack Overflow, where multiple people can give their views on a given topic, and the best ones are sorted by upvote. Except you don't need to wait for someone to ask first, and any topic goes, no matter how narrow or broad
    This feature makes it possible for readers to find better explanations of any topic created by other writers. And it allows writers to create an explanation in a place that readers might actually find it.
    Figure 1.
    Screenshot of the "Derivative" topic page
    . View it live at: ourbigbook.com/go/topic/derivative
  2. local editing: you can store all your personal knowledge base content locally in a plaintext markup format that can be edited locally and published either:
    This way you can be sure that even if OurBigBook.com were to go down one day (which we have no plans to do as it is quite cheap to host!), your content will still be perfectly readable as a static site.
    Figure 5. . You can also edit articles on the Web editor without installing anything locally.
    Video 3.
    Edit locally and publish demo
    . Source. This shows editing OurBigBook Markup and publishing it using the Visual Studio Code extension.
  3. https://raw.githubusercontent.com/ourbigbook/ourbigbook-media/master/feature/x/hilbert-space-arrow.png
  4. Infinitely deep tables of contents:
    Figure 6.
    Dynamic article tree with infinitely deep table of contents
    .
    Descendant pages can also show up as toplevel e.g.: ourbigbook.com/cirosantilli/chordate-subclade
All our software is open source and hosted at: github.com/ourbigbook/ourbigbook
Further documentation can be found at: docs.ourbigbook.com
Feel free to reach our to us for any help or suggestions: docs.ourbigbook.com/#contact