๐—”๐—ฅ๐—ข๐—ก ๐—ฆ๐—ง๐—จ๐——๐—ฌ
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ุจุณู… ุงู„ู„ู‡ ุงู„ุฑุญู…ู† ุงู„ุฑุญูŠู…

ุงู„ู„ู‡ู… ุตู„ ุนู„ู‰ ู…ุญู…ุฏ ูˆุขู„ ู…ุญู…ุฏ

ู…ุญุชูˆู‰ ุงู„ู‚ู†ุงุฉ:
ุดุฑูˆุญุงุช ุตูŠุฏู„ุฉ
ุนุถูˆูŠุฉ ู…ุฑุญู„ุฉ ุซุงู†ูŠุฉ ูƒูˆุฑุณ ุซุงู†ูŠ
ูุงุฑู…ุง ู…ุฑุญู„ุฉ ุซุงู„ุซุฉ ูƒูˆุฑุณ ุซุงู†ูŠ
ูุงุฑู…ุง ู…ุฑุญู„ุฉ ุฑุงุจุนุฉ ูƒูˆุฑุณ ุงูˆู„
ูุงุฑู…ุง ู…ุฑุญู„ุฉ ุฑุงุจุนุฉ ูƒูˆุฑุณ ุซุงู†ูŠ
ุนู„ุงุฌูŠุงุช ู…ุฑุญู„ุฉ ุฎุงู…ุณุฉ

ู„ู„ุชูˆุงุตู„:
Insta: hussian_8x

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Thiophene with..... Produced benzoyl thiophene
Anonymous Quiz
27%
Benzoyl group
20%
Acetonylacetone
53%
Benzoyl chloride
โค17๐Ÿ˜ข11๐Ÿ‘9๐Ÿ’˜9๐Ÿ‘6๐Ÿ”ฅ1
One of causes that made the pyrrole highly reactive is hetero atom that provides low electron density
Anonymous Quiz
35%
T
65%
F
๐Ÿ˜ข14๐Ÿ‘12โค9๐Ÿ‘3๐Ÿ˜2
All five-membered ring undergo sulfonation except thiophene
Anonymous Quiz
25%
T
75%
F
โค12๐Ÿ‘8๐Ÿ˜6๐Ÿ’˜3๐Ÿ‘1
1,4-diketones with Ammonium carbonate produced
Anonymous Quiz
11%
2,5 dimethyl furan
82%
2,5 dimethyl pyrrole
7%
2,5 Dimethyl thiophene
โค24๐Ÿ˜ข6๐Ÿ‘4๐Ÿ”ฅ2๐Ÿฅฐ2
Pyrrol with chloroform this reaction called
Anonymous Quiz
22%
Paal knoor reaction
78%
Reimer tieman reaction
โค20๐Ÿ˜ฑ9๐Ÿ‘5๐Ÿ’”5๐Ÿ˜4๐Ÿ˜ข3โšก1
Benzen reactivity towards electrophilic substitution higher than pyrrole
Anonymous Quiz
27%
T
73%
F
โค13๐Ÿ‘6๐Ÿ’˜5
Electrophilic substitution of thiophene occur in 2 position
Anonymous Quiz
79%
T
21%
F
๐Ÿ‘15โค7๐Ÿ˜ฑ2๐Ÿ’”1
ุงู† ุดุงุก ุงู„ู„ู‡ ู†ู„ุชู‚ูŠ ุจูƒุฑุง๐ŸŒนโค๏ธ
ุนู„ู…ูˆุฏ ู†ูƒู…ู„ ุงู„ Pyridine
โค23๐Ÿ‘17๐Ÿ’˜4
ุงู„ุณู„ุงู… ุนู„ูŠูƒู… ุดุจุงุจ
ุดู„ูˆู†ูƒู… ุงุฎุจุงุฑูƒู… ุงู† ุดุงุก ุงู„ู„ู‡ ุจุฎูŠุฑ๐Ÿค
ุนุฏู†ู‡ ูƒูˆุฒ ุน ู…ุญุงุถุฑุฉ ุงู…ุณ ู…ุณุชุนุฏูŠู†๐Ÿง
๐Ÿ‘18โค6๐Ÿ’˜4
In sulfonation reaction of pyridine is required Soโ‚ƒ
Anonymous Quiz
52%
T
48%
F
๐Ÿ‘17โค8๐Ÿ’”4๐Ÿ’˜3
๐Ÿ‘20โค8๐Ÿ’˜6๐Ÿ‘3
Electrophilic substitution reaction of pyridine occurs at
Anonymous Quiz
9%
ฮฑ position
60%
ฮฒ position
24%
ฮณ position
6%
ฮด position
๐Ÿ‘21๐Ÿ’˜6โค4๐Ÿ‘Ž3๐Ÿฅฐ3
Pyridine with CHโ‚ƒCHโ‚‚ Cl this reaction produced
Anonymous Quiz
8%
3-ethylPyridine
12%
3-chloroPyridine
70%
No. R
10%
3(Ethylchloride)Pyridine
โค17๐Ÿ‘10๐Ÿ˜ฑ4๐Ÿฅฐ3๐Ÿ’˜3๐Ÿ‘Œ2๐Ÿ‘1
Basicity of piperidine is higher than basicity of pyridine
Anonymous Quiz
72%
T
28%
F
โค16๐Ÿ‘9
Pyridine + Brโ‚‚reaction produced 3-bromo pyridine only
Anonymous Quiz
21%
T
79%
F
๐Ÿ‘14โค8๐Ÿ’˜4๐Ÿคฏ1๐Ÿ˜ญ1
Lone pair of pyridine is pyrrole like
Anonymous Quiz
22%
T
78%
F
๐Ÿ‘21๐Ÿ’˜7โค4๐Ÿ‘Ž2
Heat of combustion of pyridine is
Anonymous Quiz
7%
25kcal/mol
79%
23kcal/mol
9%
28kcal/mol
4%
3kcal/mol
๐Ÿ‘17โค7๐Ÿ’˜5๐Ÿ‘Ž2
ุจ ุงู„ ูฉ ุงู† ุดุงุก ุงู„ู„ู‡ ู†ุจู„ุด ุจู…ุญุงุถุฑุฉ ุงู„ูŠูˆู…
ูˆุฑุญ ุชูƒูˆู† ู‚ุตูŠุฑุฉ
โค21๐Ÿ‘9๐Ÿ’˜4
ุจุณู… ุงู„ู„ู‡..
โค27๐Ÿ‘6๐Ÿ’˜5๐Ÿ•Š1
Nucleophilic Substitution Reaction
ูŠุฎุถุน ู…ุฑูƒุจ ุงู„ pyridine ู„ุชูุงุนู„ุงุช ุงู„ุงุณุชุจุฏุงู„ ุงู„ู†ูŠูˆูƒู„ูŠูˆููŠู„ูŠ ุนูƒุณ ุงู„ุจู†ุฒูŠู† ูˆุงู„ุณุจุจ ู‡ูˆ

because the ring has lower electron density than benzene due to electron
withdrawal by nitrogen

ู„ุงู† ุญู„ู‚ุฉ ุงู„ pyridine ุนุฏู‡ุง lower electron density ุงู‚ู„ ู…ู† ุงู„ุจู†ุฒูŠู† ุงู„ุณุจุจ ู‡ูˆ ุฐุฑุฉ ุงู„ู†ุชุฑูˆุฌูŠู† ุญุณุจ ู…ุง ูƒู„ู†ุง ุชุดุจู‡ ุงู„ nitro group ุชูƒูˆู† ู…ุฌู…ูˆุนุฉ ุณุงุญุจุฉ
electron withdrawal group
โค46๐Ÿ‘23๐Ÿ’˜10๐Ÿ‘3