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Mbabwe Schoo: ZI LE
Mbabwe Schoo: ZI LE
Mbabwe Schoo: ZI LE
l\tIARKING SCHEr~1E
"--
NOVEIVIBER 2006
CHEMISTRY 9189/1
= .
1 (a)
The potential observed when a half cell is connected L) th<Standard~ydrogen
half cell under standard conditions. '-.- f . i!1
(b) ().) L
ComposItIOn
~11"t-/\
'
~~J
. \
( a piece of filter paper soaked in)(a saturated solution o~ a simple salt '
e.g. KN03; fL \~-5..;\•.•~4:- --;OoOo 'C;\~+
.
Use
Provides a connection between the two half cells/allows ions to flow
between the cel]s without the two solutions ,:rJ ..,.xing/ camp}.ete the, cit,·c. 'uit.. "v .
AW M-"f/",~~~'t ~ t\e:ek~\(,4·' V\<2.M.1;-(>I\.tt+Oo1t re-ve-·t~ ~~t-4 ~'Y\\.''lr~~ .
(iii)
(iv) silver: ~,Vs-.\;:,,\(;~, 'il.,;:'\i 'i""':"':')';-"" ''':.':·\..~d;,''''''~, i"; ~(':""'\i"'-., \ I' ';),'.., .. >Oo" :'"
=.;{c)
correct diagram r;j
correct conditions I 1;
i.e. Pt electrode. H2 at 1 atm ,.
H+ at 1 moldm" f- iJ-lLtit "",JIM :~l~Y
Temp 25""C/298k
[Total : 12'i
.
proceeds/titration of thiosulphate + h
fIl
Rate constant increases
the reaction)
~Lt
(ii) propanone, H€l Il.- rll
l-j
[Total:
.121
",
.
G 728 .,
(Hi) - = -- = -364KJmoT"
2 2
,; .' .•.-;-
!; ;
-!
"
~JJ\ /
4 (a) Strength of Van cler Waals' forces increasing; (on going down the group)
between molecules;
as the number of electrons in the molecules increase L, ~,~ At- i'~ fTlr'
//-:~ -:%..e. /_}/Io''l-'\.c/\,p_ I."V~ ! ta.:.:.--.-t:.. •.;J..:.<-.-~·
(b) chlorine - greenish/yellow gas
!,.j
(~onc H2S04 i<san oxidist,ng agent).'. it is able to oxidise
HBr and HI~o Br2 and h\but not Hel AW
Easy of oxidation of hydrogen halides increases down the group
.
1.1- ]
X = Br; I
;'o~1iaCI/ L;illfetfume~')~,-',,'
? '
.'
.~:
AICh SiCl4 PCI)
5 n, tlf) (i) NaCl MgCl2
:}, PCl5 \3J
..I-h (AI2C16)- -.--
+ 1 +2 +3 +4 +5 [11
;.'
"'"
,'[I t".l'Y'~li'
across the periodjorm + 1 fOl·~ff
i)
--~1
Al Chd- 6H2q,,~
. ~ 3+ '.
[AI(H20)6]p( .....-:;;-
..... (2)
(ii)
(iii)
: 1:21
\ '
'"~.\ '
6
6 (a) (i) Few CN- ions to initiate nucleophilic attack
since HCN is weakly ionised; .i\ ,x)
111
l. ,
" ~..
.-'Arace
\ ....• o~\CN from NaCN initiates nucleophilic attack on henooaldcbyde: r! 1
(ii)
'lTl"1'
.....
; "
;:'.,.
Nucleophilic addition f
(c) (i)
.>:
2
1t. ij
• ,
(ii)
rI' i .•
1
r:
. "
.;_--._i!-
HO
\,
~c~~
1\10~'-'
1 '-' 10'.·..
~)
H ll]
7 (a)
"
NH-)
I -
I
!
lC)
'-~QJl
Ethylamine
The ethyl group has an electron
L!~ 1J
releasing inductive effect /+1
.- , Ammonia
Hydrogens in ammonia are neither electron donating or withdrawing: ,.\\\ ll]
fhenylall1ine
The electrons on the nitrogcns deloC<1his s into the rng s:
//,.J!,."'y/ /;/'/~ .: <. ,', "'."!": ..',:,,,.,,
Ethanal'nide '
.s
,I
The electron withdrawing effect of the oxygen reduces the - ve
~~~~rge on the amilo nitrogen atom (hence ethanmride is
iHte basic/neutra¥jtone pair on ~~ r 1 -1
l' I
form part of a dtlocalised system of rr bonds
/ 'C _
\L 1\~ J
Sn + concHCl {renux1 Fe + con Hel
(b) (i) / "
(ii)
~-
f~'C'v~··1.c:. 'v',r_
.
/
(iii) Temperatures 0 - lOoC/
Compounds must be kept in solution
(iv)
(v)
Coupling/electrophilic substitution r1 .!
~'rotHl . 1 ',,;:.';
(ii)
CH~
~C\'H
lQJI C02H,
.
! {-C---I-{
H-C--H !
i
\ H,C:- (=--(=H.~
I-LC- C-- CE. , I '
" \)
H
H
, I.
i: !
(c) soluble; ,,' "", ,,' ,-, "" " ..~,~;,.-,,~-\>"<'
carboxyl group can hydrogen bond with water;
;; 1, !,
(d) (i)
.
I I
HC-C-CH,
3 \ • n3
uC-n-CP
\'3
:
H--C-H H-C-H
l
'1
Ii,
fll- " ry Il
H--C-C
rtl
\ ~O-CH,>CH<
CH ~ J
3
[~J'1
[Total: 121
-'