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Study Guide and Student S Solutions Manual For Organic Chemistry Pearson New International Edition Paula Y. Bruice

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Pearson New International Edition

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.BOVBMGPS0SHBOJD$IFNJTUSZ
1BVMB:#SVJDF
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Pearson Education Limited
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A catalogue record for this book is available from the British Library

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P E A R S O N C U S T O M L I B R A R Y

Table of Contents

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This page intentionally left blank
Spectroscopy Problems

1. Determine the structure of the straight-chain pentanol that produces the mass spectrum shown here.
45
100

80
Relative Intensity

60

40

20 55

73

0
10 20 30 40 50 60 70 80
m/z

2. The mass spectrum of an ether is shown here. Determine the molecular formula of the ether that would
produce this spectrum and then draw possible structures for it.

31
100

80
59
Relative Intensity

60

45 74
40

20

0
10 15 20 25 30 35 40 45 50 55 60 65 70 75
m/z

From Spectroscopy Problems of Study Guide and Solutions Manual for Organic Chemistry, Seventh Edition. Paula Yurkanis Bruice.
Copyright © 2014 by Pearson Education, Inc. All rights reserved.


Spectroscopy Problems

3. The mass spectra of pentane and isopentane are shown here. Determine which spectrum belongs to which
compound.
43
100

80
Relative Intensity

60

40

29 57
20 72

0
10 15 20 25 30 35 40 45 50 55 60 65 70 75
m/z

43
100 57

80
Relative Intensity

29
60

40

20 72

0
10 20 30 40 50 60 70 80 90 100 110 120
m/z


Spectroscopy Problems

4. Which of the following compounds gives the mass spectrum shown here?

N O
O H2N

58
100

80
Relative Intensity

60

40

44 73
20

0
10 15 20 25 30 35 40 45 50 55 60 65 70 75
m/z

5. An unknown acid underwent a reaction with 1-butanol. The product of the reaction gave the mass spectrum
shown here. What is the product of the reaction, and what acid was used?
57
100

80
Relative Intensity

41
60

40

20
136 138

0
25 50 75 100 125
m/z


Spectroscopy Problems

6. Identify the compound with molecular formula C9H10O3 that gives the following IR and 1H NMR spectra.

1
3
10 9

2
2

8 7 6 5 4 3 2 1 0
100 0.0

90 0.05

80 0.1

70
A
% B
T 0.2
60 S
R O
A R
50 N 0.3
B
S A
M N
40 I 0.4
C
T E
30 T 0.5
A 0.6
N
20 C 0.7
E 0.8
0.9
10 1.0

0 2.0
4000 3800 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1600 1400 1200 1000 800 600 450
WAVENUMBERS

7. Identify the compound with molecular formula C5H11Br that gives the following 1H NMR spectrum.

6
2 1

8 7 6 5 4 3 2 1 0


Spectroscopy Problems

8. Identify the compound with molecular formula C6H12O that gives the following IR and 1H NMR spectra.

9 8 7 6 5 4 3 2 1 0
100 0.0

90 0.05

80 0.1

70
A
% B 0.2
60 T S
R O
A R
50 N B 0.3
S A
40 M N 0.4
I C
T E
30 T 0.5
A 0.6
N
20 C 0.7
E 0.8
0.9
10 1.0

0 2.0
4000 3800 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1600 1400 1200 1000 800 600 450
WAVENUMBERS

9. A methyl-substituted benzene is treated with Cl2 in the presence of AlCl3, and a 1H NMR spectrum is taken
of one of the monochlorinated products that is isolated from the reaction mixture. Identify this compound.

2 2

8 7 6 5 4 3 2 1


Spectroscopy Problems

10. Identify the compound with molecular formula C6H14O that gives the following IR and 1H NMR spectra.

~1.5 ~0.9 41 3 6

7 6 5 4 3 2 1
100 0.0

90 0.05

80 0.1

70
%
T 0.2
60
R
A A
50 N B 0.3
S S
M O
40 I R 0.4
T B
30 T A 0.5
A N
N 0.6
C
20 C E 0.7
E 0.8
0.9
10 1.0

0 2.0
4000 3800 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1600 1400 1200 1000 800 600 450
WAVENUMBERS

11. Identify the compound with molecular formula C4H9Br that gives the following 1H NMR spectrum.

7 6 5 4 3 2 1 0


Spectroscopy Problems

12. Identify the compound with molecular formula C6H12 that gives the following IR and 1H NMR spectra.

~4.7 ~2.2 3

8 7 6 5 4 3 2 1 0
100 0.0

90 0.05

80 0.1

70
%
T 0.2
60
R
A A
50 N B 0.3
S S
M O
40 I R 0.4
T B
30 T A 0.5
A N
N 0.6
C
20 C E 0.7
E 0.8
0.9
10 1.0

0 2.0
4000 3800 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1600 1400 1200 1000 800 600 450
WAVENUMBERS

13. Identify the compound with molecular formula C8H10O that gives the following 1H NMR spectrum.

6
1
2 1
7 6 5 4 3 2 1 0


Spectroscopy Problems

14. Identify the compound with molecular formula C4H7ClO that gives the following IR and 1H NMR spectra.

8 7 6 5 4 3 2 1 0

100 0.0

90 0.05

80 0.1

70
% 0.2
60 T
R A
A B
50 N S 0.3
S O
40 M R 0.4
I B
T A
30 T N 0.5
A C 0.6
N E
20 C 0.7
E 0.8
0.9
10 1.0

0 2.0
4000 3800 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1600 1400 1200 1000 800 600 450
WAVENUMBERS

15. Identify the compound with molecular formula C8H8Br2 that gives the following 1H NMR spectrum.

8 7 6 5 4 3 2 1 0


Spectroscopy Problems

16. Identify the compound with molecular formula C4H6O that gives the following IR and 1H NMR spectra.

2 3 1

8 7 6 5 4 3 2 1 0
100 0.0

90 0.05

80 0.1

70
%
T 0.2
60 A
R B
A S
50 N O 0.3
S R
M B
40 I A 0.4
T N
30 T C 0.5
A E
N 0.6
20 C 0.7
E 0.8
0.9
10 1.0

0 2.0
4000 3800 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1600 1400 1200 1000 800 600 450
WAVENUMBERS

17. Identify the compound with molecular formula C7H8BrN that gives the following 1H NMR spectrum.

7
3

2 1
2
8 7 6 5 4 3 2 1 0


Spectroscopy Problems

18. The 1H NMR spectra of 1-chloro-3-iodopropane and 1-bromo-3-chloropropane are shown here. Which
compound gives which compound spectrum?

a.

7 6 5 4 3 2 1 0

b.

7 6 5 4 3 2 1 0

19. Identify the compound with molecular formula C4H8O that gives the following 1H NMR spectrum.

6.4 4.0 3.8

1 1 1 2 3

8 7 6 5 4 3 2 1 0


Spectroscopy Problems

20. Identify the compound with molecular formula C5H10O2 that gives the following 1H NMR spectrum.

1 3 6

8 7 6 5 4 3 2 1 0

21. Identify the compound with molecular formula C8H7O2Br that gives the following IR and 1H NMR spectra.
100 0.0

90 0.05

80 0.1

70
A
% B 0.2
60 T S
R O
A R
50 N B 0.3
S A
40 M N 0.4
I C
T E
30 T 0.5
A 0.6
N
20 C 0.7
E 0.8
0.9
10 1.0

0 2.0
4000 3800 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1600 1400 1200 1000 800 600 450
WAVENUMBERS

1
Offset: 0.4 ppm.

8 2 2 2

12 11 10 9 8 7 6 5 4 3 2 1 0


Spectroscopy Problems

22. Identify the compound with molecular formula C7H6O that gives the following 1H NMR spectrum.

2 1 2
1

10 9 8 7 6 5 4 3 2 1 0

23. The two 1H NMR spectra shown here are given by constitutional isomers with molecular formula C3H7Br.
Identify each isomer.

a.

~ 4.3

1 6

8 7 6 5 4 3 2 1 0

b.

2 2 3

8 7 6 5 4 3 2 1 0


Spectroscopy Problems

24. An unknown alkene with molecular formula C8H16 undergoes ozonolysis. Only one product is formed. The
IR and 1H NMR spectra of the product are shown here. What is the product? What alkene produced this
product?
100 0.0

90 0.05

80 0.1

70
% A 0.2
60 T B
R S
A O
50 N R 0.3
S B
40 M A 0.4
I N
T C
30 T E 0.5
A 0.6
N
20 C 0.7
E 0.8
0.9
10 1.0

0 2.0
4000 3800 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1600 1400 1200 1000 800 600 450
WAVENUMBERS

1
offset 2.5 ~2.4

1 6
7 6 5 4 3 2 1 0


Spectroscopy Problems

25. Identify the compound with molecular formula C4H7BrO2 that gives the following IR and 1H NMR spectra.
100 0.0

90 0.05

80 0.1

70
% A 0.2
60 T B
R S
A O
50 N R 0.3
S B
40 M A 0.4
I N
T C
30 T E 0.5
A 0.6
N
20 C 0.7
E 0.8
0.9
10 1.0

0 2.0
4000 3800 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1600 1400 1200 1000 800 600 450
WAVENUMBERS

offset: 0.2ppm.

12 11 10 9 8 7 6 5 4 3 2 1 0

26. Identify the compound with molecular formula C3H6Cl2 that gives the following 1H NMR spectrum.

~2.2

7 6 5 4 3 2 1 0


Spectroscopy Problems

27. A compound with the following IR spectrum was formed by a reaction with 1-propyne. If the number of
carbons in the reactant and product is the same, what compound is formed and what reaction conditions
produced this compound?

100 0.0

90 0.05

80 0.1

70
A
% B
T 0.2
60 S
R O
A R
50 N B 0.3
S A
M N
40 I 0.4
C
T E
30 T 0.5
A
N 0.6
20 C 0.7
E 0.8
0.9
10 1.0

0 2.0
4000 3800 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1600 1400 1200 1000 800 600 450
WAVENUMBERS

28. Identify the compound with molecular formula C4H8O2 that gives the following 1H and 13C NMR spectra.

CDCl3 QE-300
240 220 200 180 160 140 120 100 80 60 40 20 0

1
Offset: 0.4 ppm. ∼2.6 ppm.

1 6

12 11 10 9 8 7 6 5 4 3 2 1 0


Spectroscopy Problems

29. Identify the compound with molecular formula C4H8O2 that gives the following 1H NMR spectrum.

1
~11.8

2 2 3

6 5 4 3 2 1 0

30. Identify the compound with molecular formula C9H11NO that gives the following 1H NMR spectrum.

1 2 2 6

10 9 8 7 6 5 4 3 2 1 0

31. Identify the compound with molecular formula C9H10O2 that gives the following 1H NMR spectrum.

2
1
2 2 3

8 7 6 5 4 3 2 1 0


Spectroscopy Problems

32. The 13C NMR and 1H NMR spectra of1, 2-, 1, 3-, and 1, 4-ethylmethylbenzene are shown here. Determine
which spectrum belongs to which compound.

a. 160 140 120 100 80 60 40 20 0

Solvent

3 3 3
1 2

8 7 6 5 4 3 2 1 0

b.
160 140 120 100 80 60 40 20 0

Solvent

4 2 3 3

8 7 6 5 4 3 2 1 0


Spectroscopy Problems

c. 160 140 120 100 80 60 40 20 0

Solvent

3
4 2 3

8 7 6 5 4 3 2 1 0

33. Identify the compound with molecular formula C7H14O that gives the following 1H NMR spectrum.

~2.8 ppm

2 12

7 6 5 4 3 2 1 0


Spectroscopy Problems

34. Identify the compound with molecular formula C5H10 that gives the following 1H NMR spectrum.

8 7 6 5 4 3 2 1 0

35. Identify the compound with molecular formula C3H4O that gives the following IR and 1H NMR spectra.

2 1 1

8 7 6 5 4 3 2 1 0
100 0.0

90 0.05

80 0.1

70
% 0.2
60 T
R
A
50 N 0.3
A
S B
40 M S 0.4
I O
T R
30 T 0.5
B
A A 0.6
N N
20 C 0.7
C 0.8
E E 0.9
10 1.0

0 2.0
4000 3800 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1600 1400 1200 1000 800 600 450
WAVENUMBERS


Spectroscopy Problems

36. Identify the compound with molecular formula C4H7Cl that gives the following 1H NMR spectrum.

2
1

7 6 5 4 3 2 1 0

37. Identify the alcohol that gives the following 1H NMR spectrum.

5 2 2 1

8 7 6 5 4 3 2 1 0


Spectroscopy Problems

38. An unknown alcohol gives the following 1H NMR spectrum. Identify the alcohol. (HINT: Because this is a
spectrum of a pure alcohol, the OH proton is split by adjacent protons.)

2 6
1 1
7 6 5 4 3 2 1 0

39. Identify the compound with molecular formula C5H12O2 that gives the following 1H NMR spectrum.

7 6 5 4 3 2 1 0


Spectroscopy Problems

40. Identify the compound with molecular formula C3H7NO that gives the following IR and 1H NMR spectra.
100 0.0

90 0.05

80 0.1

70
% 0.2
60 T
R
A
50 N A 0.3
S B
M S
40 O 0.4
I
T R
30 T B 0.5
A A
N 0.6
N
20 C C 0.7
E E 0.8
0.9
10 1.0

0 2.0
4000 3800 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1600 1400 1200 1000 800 600 450
WAVENUMBERS

7 6 5 4 3 2 1 0


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nyilatkozat, a mi valaha költő szívét és tollát elhagyta.
A költő, vágyai merész röptétől elragadtatva, e költeményét bátor
volt szíve királynéjának megküldeni. Ha lelke volt a szép delnőnek,
megértheté.
Benzeráde három napig várt az eredményre. E három nap alatt
nem evett, s e három éj alatt nem aludt. Vajjon mit fog-e merész
nyilatkozatára a herczegnő válaszolni? vajjon egyáltalában
érdemesíti-e válaszra?
Harmadnap meglátogatta a költőt a herczegnő udvarmestere.
Azt az izenetet hozta neki, hogy a herczegnő óhajtana vele
titokban bizonyos ügy felől szólani.
Higyjen érzékeinek? A herczegnő titokban akar vele szólani. Érte
küldte aranyos hintaját, úgy viteti őt magához, a hátulsó lépcsőn
bocsátják fel: a titkos szeretők útján. Rejtett szőnyegajtón keresztül
vezetik be a pompás susogó szobába, melyben senki sincs más, mint
ő maga és a herczegnő.
Milyen szép volt la Valliere? az már sokszor el volt mondva.
Nekünk olyan keveset használ az, mint egykor Benzerádénak. A költő
nem bírt lélekzetéhez jönni ennyi kegy, ennyi boldogság s ennyi
csábító pompa közepett. Oh a szegény manzardlakó tudósok olyan
zavarba is jönnek mindjárt, ha egy pompás salonba vetődnek
valahogy.
La Valliere azt mondta neki, hogy űljön oda mellé. A költő nem
mert egészen mellé ülni; csak a causeuse szegletén foglalt helyet.
Akkor aztán a herczegnő maga telepedett hozzá közelebb; pompás
moir öltönyének hullámai félig eltemették a szegény szerelmes
poétát.
A herczegnő finom fehér kezével egy aranyos szélű levelkét vont
ki kebléből, a finom csipkefodrozatok közül. Oh boldog csipkék! oh
boldog papir!
Benzeráde saját sonettjére ismert abban. A boldogság egészen
elfojtá szavát.
– Kedves Benzeráde, szólt la Valliere azon a csengő hangon, a
mit a költők a seraph-zenéhez hasonlítanak, én olvastam kegyed
költeményét. Nagyon szép, gyönyörű.
Van-e költő, kit az ily kritika el ne ragadna? Szép, gyönyörű vers!
és ha ezt épen az ejti ki, a kihez czímezve van a költemény.
– Nagyon örülök, hogy önt megismertem, folytatá a bájos delnő,
olyan közel hajolva Benzerádehoz, hogy illatos lehelletét érzé arczán
s gondolkozni kezde rajta, nem volna legrövidebb útja a
paradicsomnak, most egyszerre magához ölelni azt a szép fejet, s
össze-visszacsókolni.
Még várt vele.
– Oh mi régóta keresek egy olyan igazán lángoló lelket, mint az
öné, a ki oly mélyen érezni és érzéseinek oly magas kifejezéseket
adni tudjon. Önnek minden sora egy drága gyöngyfüzér, kedves
Benzeráde; oh mint örülök, hogy önt megismerhetém. Ön nem
haragszik rám érte, hogy ide hivattam.
Benzeráde közel volt hozzá, hogy a herczegnő lábaihoz omoljon,
s a mit irásban százszor tett már, szavakban is kivallja szerelmét.
Csakhogy az a szó sokkal nehezebben jött, mint az irás.
– Én önt egy nagy szívességre kérem, folytatá la Valliere.
– Életemet! vágott közbe a költő.
– Oh azt nem, szólt mosolyogva a herczegnő. Nézze ön, mi
zavarban vagyok! Ő felsége Lajos király ezt az érzelemmel gazdag
levelet irja hozzám: olvassa ön; megengedem.
Szerelmes levél volt az la Vallierehez a királytól.
– Nekem most erre válaszolnom kellene; de én oly ügyetlen
vagyok a fogalmazásban, pedig szeretnék valami elmés, valami költői
virágokkal teljes választ küldeni a királynak, hogy bámulna rajta.
Ugy-e kedves Benzeráde, ön megteszi nekem, hogy ir egy ilyen szép,
érzelemdús viszonzást az én nevemben. Nagyon jól meg fogom adni
az árát.
Benzeráde előtt zavaros lett a világ, felugrott, elfutott; csak az
utczán vette észre, hogy kalap nélkül jött ki a herczegnőtől. Több
chansont nem irt aztán hozzá.
Szegény Benzeráde.
40.
EGY HÓHÉR.
(Iródott 1850-ben: régen múlt időben.)
Véreseknek látom a betűket magam előtt. A hóhér életrajzát
irom.
Ki annyinak adott halált, életet adok neki. Hallgassatok és féljétek
a törvény balkezét.
Jobb kezében az istennőnek a mérleg, balkezében a pallos, nem
tudhatod, ki számára van élesítve.
Amaz a biró, ez a hóhér.
Reszkess ember, midőn nevét kimondod, az a pallos.

Hajdan a hóhér nagy tiszteletben állt.


Több népnél maguk a birák hajtották végre az általuk hozott
halálitéletet… Ha most is úgy volna…
Az eutonoknál az istenek papjai, a druydák hajták végre a
véritéletet. És az elitélt kivégzése, lett legyen az bűnös, vagy
hadifogoly, áldozat volt Isten oltárán.
Az izraelitáknál a nép maga kövezte agyon elitéltjeit.
A görögök bakói a tanácsbeliek soraiban ültek. Rómában a
consulok kisérői, lictorok hajták végre a halálitéletet. Oroszországban
egyik rab végezte ki a másikat, s ki erre vállalkozott, önbüntetését
kikerülé.
Másutt vadállatok elé dobták az elitéltet, – azok ölték meg;
belevetették a vízbe, – a hullám nyelte el; – máglyára vetették, – a
láng emésztette meg; letaszíták a tarpéji szikláról, – a föld zúzta
agyon; befalazták, – az éhség vesztette el. Ki volt az, ki legelőbb
azon gondolatra jött: hogy a halálnak, a bűnök büntetésének emberi
alakot adjon? Ki teremtett legelőször embereket, kiknek neve irtózat,
hivatása életoltás, kikkel egy város árkain belől lakni irtózik a nép?
A hóhér ki van zárva az emberek köréből.
Ki szeretné őt maga mellett látni? A bűnök büntetését. Az eleven
halált?…
A hóhérnak fia is hóhér. Mi is lehetne egyéb. A szomorú hivatal
apáról fiura száll. Bele kell születni, benne kell meghalni.

Pest egyik legdíszesebb utczájában van egy csinos emeletes ház,


sok lakó van benne, mindenféle rendű és rangú emberek. A házi urat
egyik sem ismeri, a házmester nem mondja meg annak nevét… Ha
tudnák, hogy az a bakó háza!
Még két háza van azonkívül Pesten, mindenik csinos, emeletes.
A pesti bakó gazdag ember.
Többször találkoztam itt laktomban egy különös szomorú öreg
emberrel, ősz volt, mint egy galamb, haja, bajusza hófehér, s minden
vonásán valami oly szokatlan szomorúság, a minek az ember nem
talál nevet, úgy hogy midőn másodszor találkoztam vele, eszembe
jutott, hogy már egyszer láttam valahol, pedig nagy városban az
ember nem igen szokta egymást észrevenni. – Egyszer megmondta
valaki, hogy azon szomorú ősz ember a hóhér. A legnevezetesebb
hóhér az országban.
Ő
Ő nem született hóhérnak, apja nem volt az. Sok ideig élt, mint
tisztességes kereskedő, midőn egymásután következett balesetek
hirtelen megfoszták hosszú, fáradságos évek alatt szerzett
vagyonától. Ekkor elment a franczia háborúba, mint markotányos.
Oda volt, míg az egyesült seregek Párist elfoglalták, s mikor
visszajött, szorgalomgyűjtött vagyona helyébe új kincseket hozott,
mik az elvesztetteket tizszeresen múlták fölül.
De az új kincsekkel új szenvedélyeket is szerze, mik néhány év
alatt ismét mindenéből kipusztíták. Ekkor megszerette előde leányát,
a pesti bakóét. A szerelem mindenható, azzá teremti az embert, a
mivé akarja, belőle bakót teremtett.
Nejének atyja beavatta vejét műtitkaiba s nem sokára
Fehérvárott egy híres rablót itéltek halálra, kinek népi neve volt
«görbe orrú Ferke». Ezen kellett első próbáját tenni az új hóhér-
legénynek.
A rabló nagy magas férfi volt, híres neves zsivány három
vármegyében, fekete szakálla leért az öveig, s merész arcza nagy
sas-orrával egy festő mintájául szolgálhatott volna.
A rabló a vesztőhelyen épületes beszédet tartott az összegyűlt
néphez, inté a szülőket, a kik jelen voltak, hogy gyermekeiket
neveljék istenfélelemben, s okuljanak az ő szomorú sorsából, az új
bakó pedig egy csapással úgy leütötte fejét, hogy a néző közönség
villanni sem látta a pallost, csak azt látta, a mint a vér fölugrott.
Mind a rabló beszéde, mind a bakó művészete tökéletesen
megnyerte a közönség tetszését, két hétig csak ő róla beszéltek s
azontúl az új bakó híre meg volt alapítva…

A múlt évben már ősz, aggott ember volt a bakó. – Hogy tudott
így megőszülni?

Ő
Ő volt az, ki a szabadságharcz martyrjait kivégezé, –
valamennyit.
Azóta még szomorúbb lett. Napról-napra pusztult, fogyott. Nem
sokára meg is halt bele.
Egyetlen leánya maradt. Soha sem lakott az apai háznál. Nem
tudott apjával beszélni… Ki tudná megcsókolni azt a kezet, mely
irgalmat nem osztott soha, csak halált, csak büntetést? Megürült
hivatala nem maradt soká betöltetlen. Többen folyamodtak érte,
mint egy megürült püspökségért.
Az emberek czivilizálódnak.
Lábjegyzetek.
1) A régi rómaiak idejében is élt már az a hit, hogy a hüvelykujj
elvágása által a férfi elveszti bátorságát, ezért a csatából
megfutóknak hüvelykét szokták levágni; innen támadt e szó:
«poltron» a gyávák elnevezéseül (pollex troncatus).
2) E növényt még a komoly Európa legkomolyabb nemzete is
királynénak nevezte el: Victoria regia. Eddigelé csak fejedelmi
aquariumok képesek azt felmutatni.
TARTALOM.
Első kötet.

1. Százszorszépek 1
2. A láthatlan seb 17
3. Cseréljünk vőlegényt 30
4. Beczkó felesége 35
5. A székely adott szava 37
6. Egy női szó 39
7. Biró uram itélete 45
8. A fiuidoni harcz 50
9. Bebe 54
10. Két légyott 60
11. A kassai biró 62
12. Bölcs Hamlet 77
13. Faustina 88
14. Katonadolog 93
15. A hold 96
16. Sylvester éjszakák 102
17. Velezke 109
18. Kinek a halottja? 114
19. Szörnyű nemesis 117
20. A régiségbuvár 118
21. A csillagos szoba 126
22. Egy haramia-banda a havason 131
23. A megölt ország 143
24. Valdivia 156
25. A mennyei parittyakövek 181
26. Jordaki feje 193
27. Én lehettem volna az 202
28. Régi hű szerető 208
29. Karácsonyi dolgozó 214
30. Egy komondor naplója 223
31. Még egy csókot 234
32. A peregrinus 238
33. Az áruló gyűrű 255
34. Mátyás király fája 267
35. Az achæmenidion 284
36. Arria 293
37. Melyiket a kilencz közül 297
38. Abu József 303
39. Benzeráde szerelme 307
40. Egy hóhér 310

FRANKLIN-TÁRSULAT NYOMDÁJA.

Javítások.

Az eredeti szöveg helyesírásán nem változtattunk.


A nyomdai hibákat javítottuk. Ezek listája:

30 az Isten. az Isten.»
163 hallgatás tndományával hallgatás tudományával
168 átölte a gyönyörű átölelte a gyönyörű
181 31. 25.
208 29. 28.
251 Ö nem Ő nem
280 kiraly saját király saját
311 Egyszer meg. mondta Egyszer megmondta
311 hóhér- A hóhér. A
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