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the claim
Tetrahydrofuran is a stronger Lewis base than diethyl ether
the verdict
SUPPORTED
the evidence backs this
refutedsupported
the weight of evidence
2 sources for · 0 against
AS REPORTEDno primary record reached; this is what the reporting says

An organic chemistry reference source reports that tetrahydrofuran is a stronger Lewis base than diethyl ether.

Evidence for · 2
2006 · cited by 0
THF is used rather than diethyl ether. THF is a stronger Lewis base than diethyl ether, and the extra coordination … of the Ether Solvent? The oxygen of the ether is a Lewis base, and Mg is a Lewis acid. The ether donates … Li(0) , diethyl ether i hexane 10.5 Cl Li(O) , diethyl ether ee aoe hexane Li(0) , diethyl ether I ; hexane
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The analysis

rails:sufficiency:supported:single_source:for=1+1p:against=0+0p | v55:sufficiency

More for · 1
cited by 0
of ether peroxides are the reason that diethyl ether and other peroxide forming ethers like tetrahydrofuran (THF) or ethylene glycol dimethyl ether (1 In organic chemistry, ethers are a class of compounds that contain an ether group, a single oxygen atom bonded to two separate carbon atoms, each part of an organyl group (e.g., alkyl or aryl). They have the general formula R−O−R′, where R and R′ represent the organyl groups. Ethers can again be classified into two varieties: if the organyl groups are the same on both sides of the oxygen atom, the Ethers serve as Lewis bases. For instance, diethyl ether forms a complex with boron trifluoride, i.e. borane diethyl etherate (BF3·O(CH2CH3)2). Ethers also coordinate to the Mg center in Grignard reagents. Tetrahydrofuran is more basic than acyclic ethers. It forms with many complexes.
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  1. Organic chemistryreferenceno side taken
  2. Etherreferenceno side taken
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