Полезное:
Как сделать разговор полезным и приятным
Как сделать объемную звезду своими руками
Как сделать то, что делать не хочется?
Как сделать погремушку
Как сделать так чтобы женщины сами знакомились с вами
Как сделать идею коммерческой
Как сделать хорошую растяжку ног?
Как сделать наш разум здоровым?
Как сделать, чтобы люди обманывали меньше
Вопрос 4. Как сделать так, чтобы вас уважали и ценили?
Как сделать лучше себе и другим людям
Как сделать свидание интересным?
Категории:
АрхитектураАстрономияБиологияГеографияГеологияИнформатикаИскусствоИсторияКулинарияКультураМаркетингМатематикаМедицинаМенеджментОхрана трудаПравоПроизводствоПсихологияРелигияСоциологияСпортТехникаФизикаФилософияХимияЭкологияЭкономикаЭлектроника
|
Acidity and basidity of organic compounds ⇐ ПредыдущаяСтр 3 из 3
01. Lewis acids 1. donors of positive protons 2. acceptors of positive protons 3. donors of an electronic pair 4. acceptors of an electronic pair 5. oxonium basis 02. The greatest basic properties shows 1. ethoxy ethanes 2. diethylsulfede 3. diethylamines 4. ethylamine 5. triethylamine 03. The more Ка (constant of an acidity) organic compounds 1. the acidity is higher 2. the acidity is lower 3. the basicity is higher 4. electronegativity of anion there is less 5. the stability of an ion in lead-acid center is lower 04. In order of basicity increase the compounds are arranged in a row 1. C2H5 - O – C2H5, C2H5 - S – C2H5, C2H5 - NH – C2H5 2. C2H5 - S – C2H5, C2H5 - O – C2H5, C2H5 - NH – C2H5 3. there is no right answer 4. C2H5 - NH – C2H5, C2H5 - O – C2H5, C2H5 - S – C2H5 5. C2H5 - NH – C2H5, C2H5 - S – C2H5, C2H5 - O – C2H5 05. With increase of a delocalization of a negative charge of anion 1. the acidity decreases 2. the repeatability of anion decreases 3. the acidity of compounds increases 4. the basicity of compounds is increased 5. acidities of compounds do not change 06. The Basis of Lewis are: 1. acceptors of an electronic pair 2. donors of an electronic pair 3. compounds with a free orbital 4. donors of positive protons 5. acceptors of positive protons 07 To the greatest acidic properties exhibits 1. ethanol 2. ethane thiol 3. phenol 4. paraftorophenol 5. para-aminophenol 08. Quantitatively acidity of organic compounds is valued 1. stability of an ion 2. constant of an acidity (Ка) 3. constant of a basicity (Kb) 4. С С Н+, ОН- 5. electronegativity of atom in acid center 09. The greatest basicity shows the compound below: 1. CH3– NH2
2. CH3-OH
3. CH3- NH– CH3
4. CH3- SH
5. CH3- N– CH3 | CH3
10.Bronsted-Lowry acids are 1.donor of positive protons 2.donor of electrons 3.acceptor of positive protons 4.acceptors of electrons 5.neutral molecule, in which one atom with paired electrons 11. Electron-donors functional groups 1.decrease basicity 2.decrease acidity 3.increase a stability of an ion 4.increase acidity 5.don't influence acidity 12. The greatest basicity has 1.methylamine 2.dimethylamine 3.trifluoromethylamine 4.aniline 5.para-methylaniline 13. The greater the pKa of organical compounds the 1.less the acidity 2.more the basicity 3.less the basicity 4.more the ion stability 5.more the electronegativity of ion in acid centre 14.Electronoacceptors 1.increase the acidity 2.decrease the acidity 3.increase the stability of ion 4.increase the basicity 5.there is no right answer 15. The greatest basicity shows the following compound: 1. CH3 – NH2 4. CH3OH 2. CH3 - NH – CH3 5. CH3 - SH .. 3. CH3- N – CH3 | CH3
16. The least basicity shows 1. diethylamine 2. methyl amine 3. Diethyl ether 4. diethylsulfide 5. ethanol 17. The less the Ka of the organic compound the 1. more is acidity 2. less is acidity 3. less is basicity 4. more stable the anion 5. more is electronegativity of atom in the acid centre 18.By increasing of atom polarization in acid center 1. the stability of anion decreases 2. the acidity of compound decreases 3. the basicity of compound increases 4. the acidity of compound increases 5. the delocalization of negative charge of atom decreases 19. The greatest acidity shows 1. ОН - acid 2. SH - acid 3. NH - acid 4. CH - acid 5. the compounds listed are not acids 20. The least acidic properties shows 1. ethanol 2. Diethyl ether 3. ethane thiol 4. methyl amine 5. Dimethylamine 21. The least acidity shows the following compound 1. acetic acid 2. chloroacetic acid 3. Dichloroacetic acid 4. trichloroacetic acid 5. aminoacetic acid 22. Alkenes – are the bases: 1. ammonium 2. oxonium 3. sulfonium 4. pi-bases 5. neutral
23. In the following reaction HCOOH + H2O «HCOO- + H3О+ conjugated acid is: 1. formic acid 2. water 3. formiate ion 4. hydroxonium ion 5. there is no conjugated acid in this reaction
24. In the following equation of the reacion CH3-COOH + H2O «CH3-COO- + H3O+ the base is: 1. acetic acid 2. water molecule 3. acetate ion 4. hydroxonium ion 5. there is no base in this reaction
25. In order of basicity increase the following compounds are places in the row: 1. СН3- N- CH3, CH3- NH- CH3, CH3- NH2 | CH3 2. CH3- NH2, CH3- N- CH3, CH3- NH- CH3, | CH3 3. CH3- NH- CH3, CH3- NH2, CH3- N- CH3 | CH3 4. CH3- NH2, CH3- NH- CH3, CH3- N- CH3 | CH3 5. there is no correct answer 26. The acidity of the following organic compounds decreases in the row: 1. H-COOH, CH3-COOH, CH3-CH2-COOH 2. CH3-CH2-COOH, CH3-COOH, H-COOH 3. CH3-CH2-COOH, H-COOH, CH3-COOH 4. CH3-COOH, H-COOH, CH3-CH2-COOH 5. H-COOH, CH3-CH2-COOH, CH3-COOH
27. The least basicity shows 1. diethylamine 2. methyl amine 3. Diethyl ether 4. diethylsulfide 5. ethanol 28. The less the Ka of the organic compound the 1. more is acidity 2. less is acidity 3. less is basicity 4. more stable the anion 5. more is electronegativity of atom in the acid centre 29.By increasing of atom polarization in acid center 1. the stability of anion decreases 2. the acidity of compound decreases 3. the basicity of compound increases 4. the acidity of compound increases 5. the delocalization of negative charge of atom decreases 30. The greatest acidity shows 1. ОН - acid 2. SH - acid 3. NH - acid 4. CH - acid 5. the compounds listed are not acids Date: 2015-06-08; view: 505; Нарушение авторских прав |