डबल-बॉन्ड हिंदी उपयोग और उदाहरण

"" पेप्टाइड बॉन्ड, डबल बॉन्ड से इलेक्ट्रॉन के गैर-स्थानीयकरण के कारण वास्तव में प्लानर हैं।

पेप्टाइड बॉन्ड, डबल बॉन्ड से इलेक्ट्रॉन के गैर-स्थानीयकरण के कारण वास्तव में प्लानर हैं।

डबल-बॉन्ड इसके अंग्रेजी अर्थ का उदाहरण

It is specifically nandrolone with two additional double bonds in the steroid nucleus.

Sugars with a double bonded oxygen, such as fructose and glucose, are less thermally stable and tend to caramelize when overheated, but have a lower melting point for ease of preparation.

West's most well-known discovery was the synthesis of the first ever silicon-silicon double bond in 1981, a feat which broke the so-called "double-bond rule" (which stated that main group elements below row two of the periodic table could not form double bonds).

Consistent with the double bond rule, most alkyl thioketones are unstable with respect to dimerization.

Jasmone can exist in two isomeric forms with differing geometry around the pentenyl double bond, cis-jasmone and trans-jasmone.

When used with methyl methacrylate, it leads to gel point at relatively low concentrations because of the nearly equivalent reactivities of all the double bonds involved.

It is specifically testosterone with a double bond between the C1 and C2 positions.

Many metathesis reactions with ruthenium catalysts are hampered by unwanted isomerization of the newly formed double bond, and it is believed that ruthenium [that form as a side reaction are responsible.

They differ only in the position of a double bond which is endocyclic (part of the five-membered ring) in α-cubebene, but exocyclic in β-cubebene.

Triple star systems Omega-9 fatty acids (ω−9 fatty acids or n−9 fatty acids) are a family of unsaturated fatty acids which have in common a final carbon–carbon double bond in the omega−9 position; that is, the ninth bond from the methyl end of the fatty acid.

This is both because they can be created by the human body from unsaturated fat, and are therefore not essential in the diet, and because the lack of an omega−6 double bond keeps them from participating in the reactions that form the eicosanoids.

X-ray crystallography shows that the double bonds are localized, with alternatingly long and short C-C distances within the ring.

The carbonyl is then reformed and a double bond in the benzene ring attacks the carbon atom in the pronated imine cation.