समूह -C = NOH युक्त किसी भी परिसर

oxime शब्द के हिंदी अर्थ का उदाहरण:

इसके उदाहरण अनेक ऑक्सीम हैं, जो कीटोन पर हाइड्रांक्सिल ऐमीन की क्रिया से बनते हैं।

अस्पताल में भर्ती किये जाने की जरूरत वाले लोगों में, पूर्ण रक्त गणना, सीरम इलेक्ट्रोलाइट, सी-रिएक्टिव प्रोटीन स्तर के साथ-साथ पल्स ऑक्सीमेट्री, सीने की रेडियोग्राफी और रक्त परीक्षणों और संभवतः यकृत प्रकार्य परीक्षणों—को अनुशंसित किया जाता है।

जैसा कि प्रोफेसर सैंडी लेविंसन ने पुस्तक की अपनी समीक्षा में लिखा है: "यह तामीर की उपलब्धियों का एक निशान है जो" उदार-राष्ट्रवाद "शब्द के गैर-ऑक्सीमोरोनिक प्रकृति को श्रेय देने के लिए तैयार पुस्तक को समाप्त करता है और इस तरह संभावना को स्वीकार करता है कि एक नहीं है उनके बीच चयन करने के लिए मजबूर करें।

জজজ

शव परीक्षण के परिणाम अनिर्णायक थे, लेकिन 9 जून 2010 को मृत्यु के कारण का खुलासा "ऑक्सीसोडोन (Oxycodone), ऑक्सीमोर्फोन (Oxymorphone), डायाज़िपाम/नोर्डियाज़िपाम (Diazepam/Nordiazepam) और इथेनॉल (ethanol) के मिले जुले प्रभावों से उत्पन्न एक तीव्र नशे" के रूप में किया गया।

साइटोक्रोम पी-450 सक्रियण की आवश्यकता वाले ओपियोड्स (जैसे कोडीन, डिहाइड्रोकोडीन) का इस्तेमाल शायद किसी ऐसे एजेंट के साथ किया जाना चाहिए जो रासायनिक दृष्टि से एसएसआरआई से संबंधित न हो; इसके विपरीत, वे मोर्फिन, हाइड्रोमोर्फोन, ऑक्सीमोर्फोन और किसी अन्य तरीके के लिए मुक्ति, अवशोषण, वितरण, चयापचय और उन्मूलन प्रोफाइल के हिस्सों को प्रभावित कर सकते हैं।

प्रतिबंधक दोष के अलावा एस्बेस्टॉसिस के कारण प्रसारण क्षमता और धमनीय अल्प ऑक्सीमियता में कमी कर सकती है।

oxime's Usage Examples:

CH 2 OH CH20H CH20H CH20H (CH OH) 3 -> 01 OH) 3 -> (CH OH) 3 --> (CH OH)3 CH OH CH OH CH OH CHO CHO CH:NOH CN Hexose -p Oxime -> Nitrile -> Pentose.

Wohl forms the oxime and converts it into an acetylated nitrile by means of acetic anhydride and sodium acetate; ammoniacal silver nitrate solution removes hydrocyanic acid and the resulting acetate is hydrolysed by acting with ammonia to form an amide, which is finally decomposed with sulphuric acid.

Benzophenone oxime, CeHSC (:NOH)C 6 H 5, exists only in one modification which melts at 140° C.; whereas the unsymmetrical benzophenones each yield two oximes.

Mesityl oxime, (CH 3) 2 C: CH C(: NOH)CH 3, exists in two modifications.

Soc., 18 9 8, 73, p. 35 2) as a colourless liquid by the addition of hydroxylamine hydrochloride to an aqueous solution of formaldehyde in the presence of sodium carbonate; the resulting solution was extracted with ether and the oxime hydrochloride precipitated by gaseous hydrochloric acid, the precipitate being then dissolved in water, the solution exactly neutralized and distilled.

HO N Aldoximes are generally obtained by the action of hydroxylamine hydrochloride on the aldehyde in presence of sodium carbonate; the oxime being then usually extracted from the solution by ether.

Beckmann, Ber., 1886, 1 9, p. 9 8 9; 188 7, 20, p. 2580), yielding as final products an acid-amide or anilide, thus: RC(:N OH)R'-RC(OH) :NR' ---> As regards the constitution of the oximes, two possibilities exist, namely >C: NOH, or > C' ?, and the first of these is presumably correct, since on alkylation and subsequent hydrolysis an alkyl hydroxylamine of the type NH 2 OR is obtained, and consequently it is to be presumed that in the alkylated oxime, the alkyl group is attached to oxygen, and the oxime itself therefore contains the hydroxyl group. It is to be noted that the oximes of aromatic aldehydes and of unsymmetrical aromatic ketones frequently exist in isomeric forms. This isomerism is explained by the HantzschWerner hypothesis (Ber., 1890, 23, p. II) in which the assumption is made that the three valencies of the nitrogen atom do not lie in the same plane.

The carbonyl oxygen may also be replaced by the oxime group,: N OH; thus the acids yield the hydroxamic acids, R C(OH): NOH, and the acid-amides the amidoximes, R C(NH 2): NOH.

Meyer, Ber., 1900, 33, p. 2580), and this latter compound condenses with hydroxylamine to form xanthone oxime.

The carbonyl group is not ketonic in character since it yields neither an oxime nor hydrazone.

(CH OH)3 CH OH CH OH CH OH CHO CHO CH:NOH CN Hexose -p Oxime -> Nitrile -> Pentose.

Wohl forms the oxime and converts it into an acetylated nitrile by means of acetic anhydride and sodium acetate; ammoniacal silver nitrate solution removes hydrocyanic acid and the resulting acetate is hydrolysed by acting with ammonia to form an amide, which is finally decomposed with sulphuric acid.

Benzophenone oxime, CeHSC (:NOH)C 6 H 5, exists only in one modification which melts at 140° C.; whereas the unsymmetrical benzophenones each yield two oximes.

Mesityl oxime, (CH 3) 2 C: CH C(: NOH)CH 3, exists in two modifications.

Soc., 18 9 8, 73, p. 35 2) as a colourless liquid by the addition of hydroxylamine hydrochloride to an aqueous solution of formaldehyde in the presence of sodium carbonate; the resulting solution was extracted with ether and the oxime hydrochloride precipitated by gaseous hydrochloric acid, the precipitate being then dissolved in water, the solution exactly neutralized and distilled.

HO N Aldoximes are generally obtained by the action of hydroxylamine hydrochloride on the aldehyde in presence of sodium carbonate; the oxime being then usually extracted from the solution by ether.

Beckmann, Ber., 1886, 1 9, p. 9 8 9; 188 7, 20, p. 2580), yielding as final products an acid-amide or anilide, thus: RC(:N OH)R'-RC(OH) :NR' ---> As regards the constitution of the oximes, two possibilities exist, namely >C: NOH, or > C' ?, and the first of these is presumably correct, since on alkylation and subsequent hydrolysis an alkyl hydroxylamine of the type NH 2 OR is obtained, and consequently it is to be presumed that in the alkylated oxime, the alkyl group is attached to oxygen, and the oxime itself therefore contains the hydroxyl group. It is to be noted that the oximes of aromatic aldehydes and of unsymmetrical aromatic ketones frequently exist in isomeric forms. This isomerism is explained by the HantzschWerner hypothesis (Ber., 1890, 23, p. II) in which the assumption is made that the three valencies of the nitrogen atom do not lie in the same plane.

The carbonyl oxygen may also be replaced by the oxime group,: N OH; thus the acids yield the hydroxamic acids, R C(OH): NOH, and the acid-amides the amidoximes, R C(NH 2): NOH.

Meyer, Ber., 1900, 33, p. 2580), and this latter compound condenses with hydroxylamine to form xanthone oxime.

The carbonyl group is not ketonic in character since it yields neither an oxime nor hydrazone.

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oxime's Meaning':

any compound containing the group -C=NOH