studentsrepo.um.edu.mystudentsrepo.um.edu.my/2002/4/BAB_1.pdf · —CH2 CH CH —CH2 trans ---CH2...

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Transcript of studentsrepo.um.edu.mystudentsrepo.um.edu.my/2002/4/BAB_1.pdf · —CH2 CH CH —CH2 trans ---CH2...

Page 1: studentsrepo.um.edu.mystudentsrepo.um.edu.my/2002/4/BAB_1.pdf · —CH2 CH CH —CH2 trans ---CH2 CH cis Figure 3. Configuration around peptides bonds involving proline. The peptide
Page 2: studentsrepo.um.edu.mystudentsrepo.um.edu.my/2002/4/BAB_1.pdf · —CH2 CH CH —CH2 trans ---CH2 CH cis Figure 3. Configuration around peptides bonds involving proline. The peptide
Page 3: studentsrepo.um.edu.mystudentsrepo.um.edu.my/2002/4/BAB_1.pdf · —CH2 CH CH —CH2 trans ---CH2 CH cis Figure 3. Configuration around peptides bonds involving proline. The peptide
Page 4: studentsrepo.um.edu.mystudentsrepo.um.edu.my/2002/4/BAB_1.pdf · —CH2 CH CH —CH2 trans ---CH2 CH cis Figure 3. Configuration around peptides bonds involving proline. The peptide
Page 5: studentsrepo.um.edu.mystudentsrepo.um.edu.my/2002/4/BAB_1.pdf · —CH2 CH CH —CH2 trans ---CH2 CH cis Figure 3. Configuration around peptides bonds involving proline. The peptide
Page 6: studentsrepo.um.edu.mystudentsrepo.um.edu.my/2002/4/BAB_1.pdf · —CH2 CH CH —CH2 trans ---CH2 CH cis Figure 3. Configuration around peptides bonds involving proline. The peptide
Page 7: studentsrepo.um.edu.mystudentsrepo.um.edu.my/2002/4/BAB_1.pdf · —CH2 CH CH —CH2 trans ---CH2 CH cis Figure 3. Configuration around peptides bonds involving proline. The peptide
Page 8: studentsrepo.um.edu.mystudentsrepo.um.edu.my/2002/4/BAB_1.pdf · —CH2 CH CH —CH2 trans ---CH2 CH cis Figure 3. Configuration around peptides bonds involving proline. The peptide
Page 9: studentsrepo.um.edu.mystudentsrepo.um.edu.my/2002/4/BAB_1.pdf · —CH2 CH CH —CH2 trans ---CH2 CH cis Figure 3. Configuration around peptides bonds involving proline. The peptide
Page 10: studentsrepo.um.edu.mystudentsrepo.um.edu.my/2002/4/BAB_1.pdf · —CH2 CH CH —CH2 trans ---CH2 CH cis Figure 3. Configuration around peptides bonds involving proline. The peptide

RMN SPECTRES EXERCICESpcpagnol.free.fr/CRIADO/CLASSE_4/documents/documents...CH3-CH2-C—CH2-CH3 C CH—CH3 CH3-C—CH2-CH2-CH3 a. Nommer ces trois molécu es et préciser leur fonct

RMN SPECTRES EXERCICESpcpagnol.free.fr/CRIADO/CLASSE_4/documents/documents...CH3-CH2-C—CH2-CH3 C CH—CH3 CH3-C—CH2-CH2-CH3 a. Nommer ces trois molécu es et préciser leur fonct

( CH CH) · 2013. 12. 19. · (1)Nylon (ⅰ) Nylon-6 (polycaprolactam) - produced by polymerization of caprolactam (condensation reaction). NH-CH2 CH2 CO 4 N CH2 C O 5 n (ⅱ) Nylon-6,6

( CH CH) · 2013. 12. 19. · (1)Nylon (ⅰ) Nylon-6 (polycaprolactam) - produced by polymerization of caprolactam (condensation reaction). NH-CH2 CH2 CO 4 N CH2 C O 5 n (ⅱ) Nylon-6,6

OGLJIKOVODIKI - studentski.netstudentski.net/get/ulj_fkt_kt1_ok1_sno_ogljikovodiki_01.pdf · Primer : izomere heksana CH3 CH2 CH2 CH2 CH2 CH3 normalni heksan, nheksan ... 2 CH3 CH

OGLJIKOVODIKI - studentski.netstudentski.net/get/ulj_fkt_kt1_ok1_sno_ogljikovodiki_01.pdf · Primer : izomere heksana CH3 CH2 CH2 CH2 CH2 CH3 normalni heksan, nheksan ... 2 CH3 CH

3CH2 CH2 CH=CH2 3 CH2 C CH 3 2CH C CH 2 CH2 · A compound C 5 H 8 which give white ppt with ammonical AgNO 3. A give (CH 3) 2 CHCOOH with acidic K 2 Cr 2 O 7 then compound is (A)

3CH2 CH2 CH=CH2 3 CH2 C CH 3 2CH C CH 2 CH2 · A compound C 5 H 8 which give white ppt with ammonical AgNO 3. A give (CH 3) 2 CHCOOH with acidic K 2 Cr 2 O 7 then compound is (A)

CHAPTER 16-2 · 2013-12-19 · CHAPTER 16-2 Polymer Blends (reference) 1. Polymer-polymer Miscibility ... (CH2)5 CO n CH2 C H O hydrogenbonding Cl n PVC CH2 CH2 O CH2 CH2 O CH 3 CH2

CHAPTER 16-2 · 2013-12-19 · CHAPTER 16-2 Polymer Blends (reference) 1. Polymer-polymer Miscibility ... (CH2)5 CO n CH2 C H O hydrogenbonding Cl n PVC CH2 CH2 O CH2 CH2 O CH 3 CH2

Fourth Edition Chapter 6 - USP · H3C —HC 1-13C —HC H3C— C—CH CH 1-13C CH2 CH2 CH2 CH H3C—C In bacteriochlorophyll a Mg HC c=o o CH3 In chlorophyll b CH2CH3 CH3 o CH2 CH2

Fourth Edition Chapter 6 - USP · H3C —HC 1-13C —HC H3C— C—CH CH 1-13C CH2 CH2 CH2 CH H3C—C In bacteriochlorophyll a Mg HC c=o o CH3 In chlorophyll b CH2CH3 CH3 o CH2 CH2

Enzyme Applications in Pulp and Paper...(CH2)15 CH3 (CH2)15 CH3 CH 2 –----- CH–-----CH 2 . Endo-Beta 1,4 Xylanase Deinking • Paper recycling inks and stickies attach to fibers

Enzyme Applications in Pulp and Paper...(CH2)15 CH3 (CH2)15 CH3 CH 2 –----- CH–-----CH 2 . Endo-Beta 1,4 Xylanase Deinking • Paper recycling inks and stickies attach to fibers

3as.ency-education.com MH2-CH2-COOH 2,34 9,60 C 18 : C18 :1A9 MI = 127 pKa .11 Tyr NHŽ-CH-COOH OH 2,20 9,11 Asp CH-COOH CH2 COOH 1,88 3,66 NH2 Lys -CH-COOH (CH2)4 NH2 2,18 8,95 10,53

3as.ency-education.com MH2-CH2-COOH 2,34 9,60 C 18 : C18 :1A9 MI = 127 pKa .11 Tyr NHŽ-CH-COOH OH 2,20 9,11 Asp CH-COOH CH2 COOH 1,88 3,66 NH2 Lys -CH-COOH (CH2)4 NH2 2,18 8,95 10,53

spectra. - publications.iupac.orgpublications.iupac.org/pac-2007/1981/pdf/5302x0385.pdf · -CH2—CHC1—CH—CH2C1 —CH2—CC1—CH2-CH2C1 —CH2—CC1—CH2—CHC1—CH2—CH2C1

spectra. - publications.iupac.orgpublications.iupac.org/pac-2007/1981/pdf/5302x0385.pdf · -CH2—CHC1—CH—CH2C1 —CH2—CC1—CH2-CH2C1 —CH2—CC1—CH2—CHC1—CH2—CH2C1

Introduction - Chiang Mai University · isoelectric point (ppIIpI)))) ( "ˆ& $ I ... Glycylalanylvaline H3N CH2 C O CH3 NH CH C O O Glycylalanine H3N CH2 C O CH3 NH CH C O HC NH CH

Introduction - Chiang Mai University · isoelectric point (ppIIpI)))) ( "ˆ& $ I ... Glycylalanylvaline H3N CH2 C O CH3 NH CH C O O Glycylalanine H3N CH2 C O CH3 NH CH C O HC NH CH

NEG and NIOSH Basis for an Occupational Health Standarddipropylene glycol monomethyl ether, dipropylene glycol methyl ether, DPGME c7 h 1 6 3 ch3- o ch 3 ch2 - CH - O OH ch2- ch -ch

NEG and NIOSH Basis for an Occupational Health Standarddipropylene glycol monomethyl ether, dipropylene glycol methyl ether, DPGME c7 h 1 6 3 ch3- o ch 3 ch2 - CH - O OH ch2- ch -ch

Ω …Ée AÉKÓãdG ÉjQƒdÉμH 22 ``g 1434 á«fÉãdG iOɪL26`d ≥aGƒŸG · (CH2)2 pKa 2.38 1.88 07) Asp Lys (CH3)2CH - CH2 - CH - COOH NH2 HOOC - - CH - COOH NH2 H2N - (CH2)4

Ω …Ée AÉKÓãdG ÉjQƒdÉμH 22 ``g 1434 á«fÉãdG iOɪL26`d ≥aGƒŸG · (CH2)2 pKa 2.38 1.88 07) Asp Lys (CH3)2CH - CH2 - CH - COOH NH2 HOOC - - CH - COOH NH2 H2N - (CH2)4

(CH3)2C=CH2 CH3 CH2 CH3 2 H C C H CH H 3 · CH2=CHCH 2CH3 (CH 3) C=CH =CHCH 1-butene metilpropene 1-eptene 2-metil-2-eptene (CH3)2C=CHCH2CH2CH2CH3 1-cloro-1-butene C C Cl HH CH 2

(CH3)2C=CH2 CH3 CH2 CH3 2 H C C H CH H 3 · CH2=CHCH 2CH3 (CH 3) C=CH =CHCH 1-butene metilpropene 1-eptene 2-metil-2-eptene (CH3)2C=CHCH2CH2CH2CH3 1-cloro-1-butene C C Cl HH CH 2

Regulation of Leucine Catabolism in Pseudomonasputida · leucinecatabolisminp. putida (h3 h3c-ch s2ch hc-nh2 ch3 ch3 ch3 cooh h3c-ch h3c--ch h3c-c l leucine ch2 ch2 ch

Regulation of Leucine Catabolism in Pseudomonasputida · leucinecatabolisminp. putida (h3 h3c-ch s2ch hc-nh2 ch3 ch3 ch3 cooh h3c-ch h3c--ch h3c-c l leucine ch2 ch2 ch

KM C654e-20181226102959 mondai... · 2020. 3. 3. · hi 20 — —cooh nh2 ch2 ch2 ch2 —cooh nh2 —ch — nh2 cooh c=o nh2—ch— cooh ni-12—ch— cooh (3) [*11d5 (6) &

KM C654e-20181226102959 mondai... · 2020. 3. 3. · hi 20 — —cooh nh2 ch2 ch2 ch2 —cooh nh2 —ch — nh2 cooh c=o nh2—ch— cooh ni-12—ch— cooh (3) [*11d5 (6) &

Chapter 16 Arenes - Yazd...Preparation of alkenylbenzenes. Conjugation with ring KOH calc). O -CH—CH3 Cl I - I -chloroethane heat O CH=CH2 Styrene O CH=CH2 Styrene heat O CH--CH3

Chapter 16 Arenes - Yazd...Preparation of alkenylbenzenes. Conjugation with ring KOH calc). O -CH—CH3 Cl I - I -chloroethane heat O CH=CH2 Styrene O CH=CH2 Styrene heat O CH--CH3

Mgt Control System Ch 1-Ch2 Newest

Mgt Control System Ch 1-Ch2 Newest

CH3 H H CH3 H H H H H H CH2—CH3 · c) e) a ó cl ^ cl chg ch d) cha—chg á ch, f) /ch2 ch ^ ch ch2 \ch^ ch ch \ ch3 ch, ch9 4. compostos oxigenats i 5. compostos nitrogenats (pág.

CH3 H H CH3 H H H H H H CH2—CH3 · c) e) a ó cl ^ cl chg ch d) cha—chg á ch, f) /ch2 ch ^ ch ch2 \ch^ ch ch \ ch3 ch, ch9 4. compostos oxigenats i 5. compostos nitrogenats (pág.

Ch2 New formatted 020114 ch HR links - manual-solution.com

Ch2 New formatted 020114 ch HR links - manual-solution.com

SSA ALPINE CH 1, CH2

SSA ALPINE CH 1, CH2