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2. File:Di-tert-butyl ether chemical structure.svg - Wikipedia

   en.wikipedia.org/wiki/File:Di-tert-butyl_ether...

   Printable version; Page information; Get shortened URL; Download QR code; In other projects Appearance. ... Di-tert-butyl ether chemical structure: Date: 22 April 2007:

3. Di-tert-butyl ether - Wikipedia

   en.wikipedia.org/wiki/Di-tert-butyl_ether

   Printable version; In other projects Wikimedia Commons; Wikidata item; Appearance. move to sidebar hide ... Di-tert-butyl ether is a tertiary ether, ...

4. Category:Dialkyl ethers - Wikipedia

   en.wikipedia.org/wiki/Category:Dialkyl_ethers

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5. Butyl group - Wikipedia

   en.wikipedia.org/wiki/Butyl_group

   The effect of the tert-butyl group on the progress of a chemical reaction is called the Thorpe–Ingold effect illustrated in the Diels-Alder reaction below. Compared to a hydrogen substituent, the tert-butyl substituent accelerates the reaction rate by a factor of 240. [2] tert-Butyl effect. The tert-butyl effect is an example of steric hindrance.

6. Category:Tert-butyl compounds - Wikipedia

   en.wikipedia.org/wiki/Category:Tert-butyl_compounds

   Pages in category "Tert-butyl compounds" The following 200 pages are in this category, out of approximately 203 total. This list may not reflect recent changes .

7. Category:Ether solvents - Wikipedia

   en.wikipedia.org/wiki/Category:Ether_solvents

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8. tert-Butyl alcohol - Wikipedia

   en.wikipedia.org/wiki/Tert-Butyl_alcohol

   The tert-butoxide is a strong, non-nucleophilic base in organic chemistry. It readily abstracts acidic protons from substrates, but its steric bulk inhibits the group from participating in nucleophilic substitution, such as in a Williamson ether synthesis or an S N 2 reaction. tert-Butyl alcohol reacts with hydrogen chloride to form tert-butyl ...

9. Bulky cyclopentadienyl ligands - Wikipedia

   en.wikipedia.org/wiki/Bulky_cyclopentadienyl_ligands

   The intermediate in this synthesis is di-tert-butylcyclopentadiene. This compound is conveniently prepared by alkylation of cyclobutadiene with tert-butyl bromide under phase-transfer conditions. [2] [1] Illustrative of the unusual complexes made possible with these bulky ligands is molecular iron nitrido complex (t Bu 3 C 5 H 2) 2 Fe 2 N 2. [3]