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4 Study of presence of #
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Oxalate ions |
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[ Guava Fruit |
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the guidetines by CBSE..
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This is to costify that PRITENDRA SINGH TIWARI class 12!
KENDRIYA VIDYALAYA NO2 REWALMP] . has successfully
completed his project work in chemistry on the topie-
“PRESENCE OF OXALATE JONS IN GUAVA FRUIT AT DIFFERENT
STAGES OF RIPENING’
HE has taken proper care and shown at most
a sincerity in completion of this project uo to my expectation and ag per
Signature of principle
IMISSSEEMA TAMRAKAR} IDRAJAY SINGH]
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S.No. Topic Page !
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I 1. | Acknowledgement 4 J
| 2. | Introduction 6 #
L 3. |Plant Chemicals —_|6 j
% 4. |Oxalic Acid 8 &
* 5. | Experiment 9 *
i 6. | Observations ul 4
i 7. | Calculations 12 4
i 8. | Conclusion 13 ji
[ 9. | Bibliography 14 i
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ACKNOWLEDGEMENT 4
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At the outset , J express my heartiest gratitude to &
my guide “MISS.SEEMA TAMRAKAR’ for the ry
divine guidance and wisdom showered on me to #
undertake this project. i
7 am immensely grateful to
my Geloved Principal for his involvement in this 4
project by providing useful inputs and timely «
suggestion. x
My parents also played a key P|
role in shaping up this project nicely and J convey !
wy special thanks to them as well. "|
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¢& INTRODUCTION
& Famity: Myrtaccac
Genus: Psidiun
Species: guajava
& Common names: Guava, goiaba, guayaba, djamboe, diambu,
goavier, gouyave, goyave, goyavier, perata, Gayawas, dipajaya
jambu, petokal, tokal, guave, guavenbaum, guayave, Ganjiro,
& goiabeiro, guayabo, guyaba, gocajaaba, guave, goojaba,
uawa, abas, jambu batu, bayabas, pichi, posh, enandi
Part Used: Fruit, Coaf, bark
Guava ig a common ghade tree or shrub in dooryard gardens in
the tropics. It provides shade while the guava [ruils are eaten
& fresh and made into drinks, ice cream, and preserves. In the
richness of the Amazon, guava fruits often grow well beyond
the size of tennis Gales on well-Granched trees or shrubs
8 reaching up to 20 m high. Cultivated varictics average about 10
| motors in height and produce Comon-sized fruits. The tree ig
easily identified by its distinctive thin, smooth, copper-colored
Gark that flakes off, showing a greenish layer Gencath,
Guava frnit today is considered minor in terms of commercial
wored trade but is widely grown in the tropics, enriching the dict
of hundreds of millions of people in the tropics of the wored.
& Guava hag spread widely throughout the tropics Gecauge it
| thrives in a variety of soils, propagates cagity, and Gears fruit
rolatively quickly. The fruits contain numerous seeds that can
produce a mature fruit-Gearing plant within four years.SO
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é PLANT CHEMICALS
Guava is tich in tannins, phenols, triterpenes, flavonoids, essential oils,
saponins, carotenoids, lectins, vitamins, fiber and fatty acids. Guava feult
is higher in vitamin C than citrus (80 mg of vitasmln @ ix 100 9 of fred)
and contain appreciable amounts of vitamin A as well. Guava fruits
are also a good source of pectin - a dictary fiber. The Leaves of guava are
ich in flavonoids, in particular, quercetin. Much of guava's therapeutic
activity is attriduted to these (Lavonoids. The flavonoids have
demonstrated antiGactorial activity. Quercetin ig thought to contribute to
the anti-diarrhea offect of guava; it ig able to relax intestinal smooth
muscle and inhibit Gowel contractions. In addition, other (Cavonoids
and triterpenes in guava Caves show antispasmodic activity. Guava also
has antioxidant properties, which is attributed to the polyphenols found
in the Coaves.
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Guava's main plant chemicals include: alanine, alpha-humublenc,
alpha-hydroxyursotic acid, alpha-tinolenic acid, alpha-setinene,
amuritoside, araban, arabinose, arabopyranosides, arjunotic acid,
aromadendrene, ascorbic acid, ascorbigen, asiatic acid, aspartic acid,
avicuarin, Genzabdehyde, butanal, carotenoids, caryophyllene, catechoe-
tannins, crataegotic acid, D-galactose, D-galacturonic acid, ellagic acid,
ethyl octanoate, essential oils, fCavonoids, gallic acid, glutamic acid,
goreishic acid, guatine, guavacoumarie acid, guaijavarin, guajiverine,
guajivotic acid, guajavotide, guavenoic acid, guajavanoic acid, histidine,
Ayperin, iteCatifol igonerincoumaric acid, isoquercetin, jacoumaric acid,
becting, Coucocyaniding, Cimonene, Cinoleic acid, Cinolenic acid, lysine,
mecocyanin, myticotin, myristic acid, nerolidiot, obtusinin, octanol,
& olecanotic acid, oteic acid, oxalic acid, palmitic acid, palmitoteic acid,
pectin, polyphenols, psidiotic acid, quercetin, quercitrin, serine,
& segquiguavene, tanning, terpenes, and urgotic acid.
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Main Prepatation Mathod: decoction
Main Actions (in orden):
cardiotonic (tones, batances, strengthens the heart)
Main Uses:
1. for dysentery (acteriat and amebic?, diarrhea, cotie, and
intantite rotavirus enteritis
. as a broad-spectrum antimicrobiag for internal and
infections
fo tone, Gabance, protect and strengthen the heart (and
for arrhythmia and some heart diseases)
ag a. cough suppressant, analgesic (pain-retiever), and
Febrituge (reduces fever) for cotds, feu, sore throat, ete
. asa topical remedy for ear and eye infections
Propertios/ Actions Documented by Regeasch:
amebicide, analgesic (painretiever), antibacterial, anticandidat,
antispasmodic, antiutcerons, cardiodepressant, cardiotonic
(tones, batances, strengthens the heart), contrat nervous system
depressant, cough suppressant, gastrototonic (tones, balances,
strengthens the gastric tract), Aypotensive (Cowers Good
prossure), sedative, vasoconstrictor
Other Properties/ Actions Documented by Traditional Use:
cleanser, digestive stimulant, menstrual stimuéant, nervine
Gatances/catms nerves), vermifuge (expels worms)
Casdions: It has a cardiac depressant effect and is
contraindicated in some heart conditions.
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° OH
OXALIC ACID
HO °
+ IT ig the chemical compound formula H2020s. This dicarboxylic
acid is Getter described with the formuba HO:CCO:H, It is a
relatively strong organic a cid, boing about 10,000 times stronger
than acetic acid. The dianion, gnown as oxalate, is also a reducing
agent and a tigand in coordination choinistry. Oxatic acid and
oxatates are abundantly present in many plants, most notably in
sour grass, and sorrel (including Oxatid, roots and Ceaves of
rhubar and Guckwheat.
+ At high concentrations, it is a dangerous poison, but such
immediately toxic Covels are not found in foodstuffs Gut rather in
manufactures, such as some bleaches, some anti-rust products,
and some metal clcaners (among othet things)It is also a
naturatey oteurcing component of plants; andis found in
rabntivety high¢ovees in dark-green Leafy foods)
4 In the human Gody, ingested oxatie acid is not a useful uutricnt;
80, tie ale such unneeded components of dict, it is processed by
the Gody toa jont form and that Gyproduct is thon excreted.
in this case. inthe urine. Jn the course of Geing processed by the
body, oxatic acid combines with other substances to form various
satts, talled oxabates; usually, those salts are in Solution, Gut
in high concentration some may precipitate out in crystalline form.
Such tiny crystals can cause damage to human tissue, especiatey
fo the stomach, the kidneys, and the bladder. It is commonty
Getioved that oxatates contribute to the formation of kidney and
Gladder stones; one common nutricnt with which oxatie acid
combines is calcium, making the salt calcium oxalate, and
calcium oxalate is found in Ridney stone
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§ To study the presence of Oxalate #
& Jon content in Guava Fruit at different #
* stages of ripening Yen #
HO oO
ir Requirements: /00 0 soosnring (Lash, posite and mortar, booker, 4
& titration flash, funnel, burctte, weight box, pipette, fitter paper, dieute s
4:80.54, KMun0;, and guava fruits at different stages of ripening.
& &
L Theory :Oxalate ions are extracted from the fruit by a
Goiting pulp with dit. #,S$0,, Then Oxalate ions are
ie estimated volumetrically by titrating the solution with 4
b standard KMn0, solution. #
* @ud Point: Appearance of permanent pink colour. &
& Procaduee: &
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1. 50.09 of fresh guava was weighed and crushed to a fine pulp
& using postlc-mortar. oe
2. The crushed pulp was transferred to a Beaker and about 50mé dit.
- #180, was added. The contents were Goited for about 10 minutes. &
L 5. The contents wore filtered and cooted in 100me measusing flask. A
r The volume was made up to 100me by adding disti¢éed water. “
& 4. Ome of this solution was taken into a titerating flask and 20me oe
of dit. 4:80, was added to it. The mixture was heated to about
& 60°C and titerated against the standard KMn0; solution taken in ss
4b a buette a
5. The process was repeated with different samples of guava,
% *
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CIBSERVATION
Weight of guava taken
= 50.04
Volume of guava extract taken = 20.0 me
Normatity of KMnO, solution = 1_
20
Guava
extract from
Burette
readings
Concordant
volume of
Initial) Final
KMnO,
Solution
used
Fresh
50
50
1 day old
30
30
2 day old
15
3 day old
s\is|s|s
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SP:
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Pa.
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bo 80 So Bo
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RRR
= Oo OH
Calculations" °
NW, = Nw
(guava extract) (KMn0; solution)
Nix20 = 1xv
20
Normatity of oxalate, Ni =\__
400
Strength of oxalate = Normatity x €q. mags of oxalate ion
= ein 44 g/litro of the dituted extract.
Guava Strength of
extract oxalate ion
from (gleitre)
Fresh 5.5
1 day old 3.3
2 day old 1.65
3 day old 0.99
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._ Conclusion © o +
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I Oxatic acid and oxalates are abundantly
h present in many plants, most notably in P|
h sour grass, and soree (including Oxad/s), i
I, roots and Cleaves of rhubarb and !
I Guckwheat. i
; After doing this experiment we can 5
, conclude that uncipe guava has a high 4
r content of Oxalate ions. The concentration 4
i of oxalate iong decreases with the .
ig cipening of fruit. 4
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[ BIBLIOGRAPHY i
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Tn order to complete this project, J took help
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from:
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- * My chemistry teacher *
* + Comprehensive Practical Chemistry &
* (Lab Manual) of Laxmi Publication &
uy + Different internet sites: #
A * www.google.com #
° www.rnin-tree.com
* &
¢ www.wikipedia.com
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