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Dienes and Ultraviolet Spectroscopy

Base-induced elimination of allylic halides is the most common method. [Pg.317]

The C2-C3 bond length of 1,3-butadiene is 5 pm shorter than a C-C single bond. [Pg.317]

A substituent in a bicyclic ring system is endo if it is syn to the larger of the other two bridges. [Pg.318]

Heating rubber with sulfur forms cross-links that lock the chains together, n. Ultraviolet spectroscopy (Sections 14.7 - 14.9). [Pg.318]

The eneigy absorbed is used to promote a n electron in a conjugated system from one orbital to another. [Pg.318]

Multiple bonds that alternate with single bonds are said to be conjugated. Thus, 1,3-butadiene is a conjugated diene, whereas 1,4-pentadiene is a non- conjugated diene. [Pg.522]

3-Butadiene (conjugated alternating double and single bonds) [Pg.522]

See other pages where Dienes and Ultraviolet Spectroscopy is mentioned: [Pg.317]    [Pg.319]    [Pg.321]    [Pg.323]    [Pg.325]    [Pg.327]    [Pg.329]    [Pg.331]    [Pg.333]    [Pg.335]    [Pg.337]    [Pg.339]    [Pg.10]    [Pg.542]    [Pg.522]    [Pg.524]    [Pg.526]    [Pg.530]    [Pg.532]    [Pg.534]    [Pg.536]    [Pg.538]    [Pg.540]    [Pg.542]    [Pg.544]    [Pg.546]    [Pg.548]    [Pg.550]    [Pg.554]    [Pg.556]    [Pg.558]    [Pg.10]    [Pg.542]    [Pg.546]    [Pg.550]    [Pg.552]    [Pg.554]    [Pg.556]    [Pg.558]    [Pg.562]    [Pg.566]    [Pg.574]    [Pg.576]    [Pg.578]    [Pg.522]    [Pg.524]    [Pg.526]   


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And dienes

Conjugated Dienes and Ultraviolet Spectroscopy

Ultraviolet spectroscopy

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