ಬಣ್ಣರಹಿತ ದಹನಕಾರಿ ಅನಿಲವನ್ನು ಮುಖ್ಯವಾಗಿ ಎರಕಹೊಯ್ದ ಮತ್ತು ಜೈವಿಕ ಸಂಶ್ಲೇಷಣೆಯಲ್ಲಿ ಬಳಸಲಾಗುತ್ತದೆ,

alkynes ಕನ್ನಡದಲ್ಲಿ ಉದಾಹರಣೆ:

ತ್ರ್ರಿಬಂಧವುಳ್ಳ ಆ್ಯಲಿಫ್ಯಾಟಿಕ್ ಸಂಯುಕ್ತಗಳು ಅಸಿಟಲೀನ್ ಅಥವಾ ಆಲ್ಕೈನ್ಗಳು.

alkynes's Usage Examples:

Aliphatic compounds can be saturated, joined by single bonds (alkanes), or unsaturated, with double bonds (alkenes) or triple bonds (alkynes).

With unsymmetrical alkenes or alkynes, regioselectivity can be problematic, but less so.

The reaction of alkynes are similar, with the product being a geminal dihalide; once again, Markovnikov"s.

Urushibara Nickel, an nickel based catalyst used to hydrogenate alkynes to alkenes.

4-octyne (dipropylethin) and 3-hexyne (diethylethin) a group of symmetric alkynes.

Unsaturated compounds, especially alkenes and alkynes, add halogens: RCHCHR′ + X2 → RCHX–CHXR′ In oxychlorination.

Addition reactions apply to alkenes and alkynes.

The acidic hydrogen on terminal alkynes can be replaced by a variety of groups resulting.

phosphaalkynes, isocyanides, carbon monoxide, dinitrogen, nitriles, cyanamides, nitric oxide, oximes, oxadiazolines, carboxamides, amidines, olefins.

The hexynes are a subgroup from the group of alkynes.

The name comes from mix of propene and argentum, which refers to the typical reaction of the terminal alkynes.

hydrochlorinations of alkynes in producing the chlorinated monomers chloroprene and vinyl chloride, which are subsequently polymerized to make polychloroprene.

Alkenes and alkynes form organic compounds in which the multiple.