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"Mony Mony" was the only song by the group to reach the top 20 in the United Kingdom; it reached No. 1 in the UK, [4] No. 3 in the U.S. and Canada, and became a Top 10 hit across western Europe. A music video was made featuring the band performing the song amidst psychedelic backgrounds. A decade and a half later, it would receive renewed play ...
1,3-Diols are described as syn or anti depending on the relative stereochemistries of the carbon atoms bearing the hydroxyl functional groups. Zincophorin is a natural product that contains both syn and anti 1,3-diols. Zincophorin depicting syn and anti-1,3-diol configurations
Thirty Three & 1 ⁄ 3 (stylised as Thirty Three & 1 ⁄ ॐ on the album cover) is the seventh studio album by the English musician George Harrison, released in November 1976. It was Harrison's first album release on his Dark Horse record label, the worldwide distribution for which changed from A&M Records to Warner Bros. as a result of his ...
a 1,3-diol (1,3-Propanediol, middle) and a 1,4-diol (1,4-Butanediol, bottom). An alkanediol, composed of alkane and diol, are a group of substances consisting of linear or branched hydrocarbon chains containing exactly two hydroxy groups at different positions. They are a subgroup of the diols and contain no other heteroatoms or multiple bonds
"1, 2, 3, Red Light" is a song written by Sal Trimachi and Bobbi Trimachi and was recorded by 1910 Fruitgum Company for their 1968 album, 1, 2, 3, Red Light. [2] The song charted highest in Canada, going to number 1 on the RPM 100 national singles chart in 1968. [3] In the same year in the US, it went to number 5 on the Billboard Hot 100 and ...
1,3-Butanediol is an organic compound with the formula CH 3 CH(OH)CH 2 CH 2 OH. With two alcohol functional groups, the molecule is classified as a diol . The compound is also chiral, but most studies do not distinguish the enantiomers.
[1,3] diols have a tendency to eliminate water following the monooxidation by Fétizon's reagent to form an enone. [8] Upon oxidation with Fetizon's reagent, a 1,3 diol may eliminate water to produce an enone. Under differing structural conditions, [1,2] diols can form diketones in the presence of Fétizon's reagent.
1,10-Decanediol is a diol compound characterized by the chemical formula C 10 H 22 O 2. 1,10-Decanediol can be synthesized through the reduction of dimethyl sebacate using sodium borohydride in an ethanol medium, with Cerium(III) chloride serving as the catalyst.