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[A 2] Of this experiment, Albert Einstein wrote, "If the Michelson–Morley experiment had not brought us into serious embarrassment, no one would have regarded the relativity theory as a (halfway) redemption." [A 3]: 219 Michelson–Morley type experiments have been repeated many times with steadily increasing sensitivity.
Luminiferous aether or ether [1] (luminiferous meaning 'light-bearing') was the postulated medium for the propagation of light. [2] It was invoked to explain the ability of the apparently wave -based light to propagate through empty space (a vacuum ), something that waves should not be able to do.
According to ancient and medieval science, aether (/ ˈ iː θ ər /, alternative spellings include æther, aither, and ether), also known as the fifth element or quintessence, is the material that fills the region of the universe beyond the terrestrial sphere. [1]
The timeline of luminiferous aether (light-bearing aether) or ether as a medium for propagating electromagnetic radiation begins in the 18th century. The aether was assumed to exist for much of the 19th century—until the Michelson–Morley experiment returned its famous null result.
In the 19th century, luminiferous aether (or ether), meaning light-bearing aether, was a theorized medium for the propagation of light. James Clerk Maxwell developed a model to explain electric and magnetic phenomena using the aether, a model that led to what are now called Maxwell's equations and the understanding that light is an ...
A big challenge for the Lorentz ether theory was the Michelson–Morley experiment in 1887. According to the theories of Fresnel and Lorentz, a relative motion to an immobile aether had to be determined by this experiment; however, the result was negative.
The general structure of an ether. R and R' represent most organyl substituents.. 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).
Ether cleavage refers to chemical substitution reactions that lead to the cleavage of ethers. Due to the high chemical stability of ethers, the cleavage of the C-O bond is uncommon in the absence of specialized reagents or under extreme conditions. [1] [2] In organic chemistry, ether cleavage is an acid catalyzed nucleophilic substitution reaction.