Examples of using Aldehyde in English and their translations into Hungarian
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The first line of defense is a family of enzymes called aldehyde dehydrogenases(ALDH) that break down harmful acetaldehyde into acetate which is utilized by our cells as a source of energy.
The first is a family of enzymes called aldehyde dehydrogenases(ALDH) which break down harmful acetaldehyde into acetate, which our cells can use as a source of energy.
Nucleophilic addition of an alcohol to a carbonyl group of an aldehyde Nucleophilic addition of an alcohol to a resonance stabilized hemiacetal cation Partial hydrolysis of an acetal.
An aldehyde dissolved in water exists in equilibrium with low concentrations of its hydrate, R-CH(OH)2.
Similarly, in excess alcohol, the aldehyde, its hemiacetal, and its acetal all exist in solution.
Perfumers can give free rein to their creativity to enrich them with green, aldehyde, fruity or spicy touches.
you may have an aldehyde problem.
One way of acetal formation is the nucleophilic addition of an alcohol to a ketone or an aldehyde.
oxygen compounds like alcohol, aldehyde, ketone, carboxylic acid,
and historically, the term acetal was used specifically for the aldehyde cases.[1] Cellulose is a ubiquitous example of an acetal.
Ammonia toxicity and aldehyde toxicity are two common findings in clinical practice
forestry carbon materials key technology""high performance wood(bamboo) mass material manufacturing technology""non aldehyde thermoplastic resin plywood manufacturing technology""all-round technology of biomass gasification," the five technologies.
Other aldehydes give secondary alcohols for this reaction,
Imidazolidines are traditionally prepared by condensation reaction of 1,2-diamines and aldehydes.
Aldehydes, are mainly found in freshly roasted coffee,
Aldehydes expressed in grams of acetaldehyde per hectolitre of alcohol at 100% vol.: 0,5.
It is quite expensive disinfection method in which the emission of harmful substances, aldehydes and ketones.
Some aldehydes are created during.
Aldehydes and derivatives(1).
The hydrogenation of polar substrates such as ketones and aldehydes typically require transfer hydrogenation,