a mix of AS topics Flashcards

1
Q

define covalent bond

explain how they occur

A

strong electrostatic attraction between a shared pair of e- and the nuclei of the bonded atoms

unpaired e- in an orbital of an atoms shared with an unpaired e- in another atom’s orbital

atoms may promote e- into previously unoccupied orbitals in the same energy level to form more covalent bond

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2
Q

define dative covalent bond

A

a covalent bond where both e- come from the same atom

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3
Q

Activation Energy

A

Minimum energy (1)
required before a reaction can occur (1)

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4
Q

disadvantage of dot and cross diagrams

A

assumes atoms within the compound are arranged along one plane only (sometimes true)

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5
Q

metallic structure and properties of metals

A

lattice of postive metal ions surrounded b sea of delocalised e-

heat conductivity due to delocalised e- being able to carry heat energy and passing it through metal cations

high density due to cations packing closely together

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6
Q

solubilty rules

A
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7
Q

expalin what determines the shape of a molecule

A

determined by arrangement of e- pairs around the central atoms which is influenced by the repuslion between the e- pairs (depends if e- pairs are BP or LP)

e- pairs repels each other to be as far apart as possible

all BP repel each other equally

LP repel more than BP because they are held closer ti the central atom

LP repel LP more than they repel BP

molecules take up the shape that minimises repulsion

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8
Q

define electronegativity

A

ability of an atom to attract e- pair in a covalent bond towards itself

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9
Q

define enthalpy change

A

heat energy change measured at a constant pressure

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10
Q

what does Hess’s law state

A

enthalpy change of reaction is independent of which route it takes

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11
Q

define mean bond enthalpy

A

energy required to break a covalent bond measured over a range of molecules containing the bond

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12
Q

define periodicity

A

pattern in the change of properties of a row of elements which is repeated across the next row

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13
Q

standard enthalpy of combustion definition

A

enthalpy change when 1 mole of a substance is completely burned in excess oxygen under standard conditions

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14
Q

standard enthalpy of formation definition

A

enthalpy change when 1 mole of a compound is formed from its constituent elements in their standard states under standard conditions

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15
Q

test for ammonium, hydroxide and sulphate ions

A

positive ion tests:

  • test for ammonium ions
    • Add dilute NaOH (aq) to sample in a test tube and gently heat
    • Dip damp litmus paper (so ammonia gas can dissolve) into test tube
    • NH3 gas produced in positive test which turns litmus paper blue as it is alkaline
    • NH4+ (aq)+ OH- (aq)⟶ NH3 (g)+ H2O (l)

test for negative ions

  • Hydroxide ions
    • as they are alkaline, either a pH meter or litmus paper can be used
    • red litmus paper turns blue in presence of OH-
  • sulphate ions
    • Add dilute HCl (to eliminate presence of CO32- ions)
    • Then add BaCl2 (aq)
    • A white precipitate of barium sulphate forms:
    • SO42-(aq)+Ba2+(aq)⟶ BaSO4(s)
  • carbonate ions
    • add dilute HCl
    • Bubble gas formed through test tube of limewater
    • effervescence and limewater turns cloudy in positive result
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16
Q

explain the trend in first IE in group 2 from Mg to Ba

A

decreases because:

  • atomic radius increases - greater distance between outermost e- and nucleus
  • shielding increases
  • both these things decrease the strength of the electrostatic atraction between the -vely charged outermost e- and the +vely charged nucleus = less energy required to overcome the attraction
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17
Q

A sample of Boron has a relative atomic mass of 10.8. the sample contains the isotopes 10B and 11B. calculate the percentage abundance of 10B in this sample

A

let the abundance of 10B be x. this means that the abundance of 11B is (100-x)
set up an equation to find x: (10x+11(100-x)) / 100 = 10.8
so 10x+1100-11x=1080
so x=20
Therefore the abundance of 10B is 20%

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18
Q

which element in period 3 will have the highest 2nd IE and why?

A

Na because the e- being removed from the Na+ is in a 2p orbital (all other elements have their outer e- in a higher energy level from 3s and above)

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19
Q

explain the overall trend of 1st IE across period 3

A

increases because:

  • no. of protons increases
  • same shielding
  • decreased atomic radius
  • results in stronger electrostatic attraction between outer e- and nucleus
  • more energy required to remove e-
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20
Q

why do Al and S have a lower than expected 1st IE

A

the outer electron of Al is in a 3p orbital rather than 3s (like Na and Mg )which is further from nucleus = more shielding from inner electrons = less energy needed to remove this electron

the 3p4 electron configuration in S means that electron lost from S is from an orbital containing a pair of e- = more repulsion between electrons in S= less energy required to remove electrons

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21
Q

explain the trend in electronegativity across period 3

A

electronegativity increases

Nuclear charge increases= more protons and same amount of shielding= decreasing atomic radius= increased electrostatic attraction between nucleus and the electron pair in the covalent bond

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22
Q

explain the trend in melting points across period 3

A

from Na to Al, ionic radius decreases and more delocalised electrons= stronger electrostatic attraction between delocalised electrons and positive metal ions = more energy required to overcome

Si has a very high melting point due to macromolecular structure - many strong covalent bonds - lots of energy needed to overcome

S8 has a higher melting point than P4 because it is a bigger molecule= more electrons= stronger Van der Waals’ forces between S8 molecules= more energy needed to separate the molecules

Ar has a very low melting point as it is monoatomic = very weak Van der Waals’ forces between the atoms= little energy needed to separate Ar atoms

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23
Q

explain the trend in atomic radius across period 3

A

decreases because:

  • bigger nuclear charge and shielding stays the same= stronger electrostatic attraction between outer electrons and nucleus= outer electrons drawn in more closely to nucleus
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24
Q

explain trend of atomic radius down group 2

A

Atomic radius increases down the group because:

there are more filled shells between the nucleus and the outer electrons

the outer electrons are more shielded from the attraction of the nucleus = weaker electrostatic attraction between -ve e- and +ve nucleus

so outer electrons are further from the nucleus

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25
Q

explain trend in 1st IE down group 2

A

First ionisation energy decreases down the group because:

Atomic radius increases= each element has one more electron shell than the previous one=more shielding = weaker electrostatic attraction between nucleus and outer electrons = less energy required to remove outer electron

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26
Q

explain trend in melting points down group 2

A

Melting point decrease down the group because:

Ionic radius increases=delocalised electrons are further away from the positive nucleus= weaker electrostatic attraction between delocalised electrons and positive 2+ ions= weaker metallic bond= less energy required to break metallic bonds

Mg is an exception to this trend because of its metallic crystalline structure - higher MP than expected

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27
Q

explain trend in reactivity with water down group 2

A

Be- no reaction, Mg reacts very slowly to produce Mg(OH)2 + H2, Ca, Sr and Ba react vigorously to form metal hydroxides + H2

With steam, Mg reacts to form MgO + water (because Mg(OH)2 is less stable at high temps)

In the reactions of Ca, Sr and Ba with water the bubbles of H2 can be seen as effervescence and a white precipitate will form. The reaction is exothermic so the solution would feel hot.

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28
Q

solubility of group 2 hydroxides/sulphates in water

A
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29
Q

Uses of group 2 compounds and elements

A
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30
Q

shapes of molecules

A

presence of LP reduces bond angle by 2.5º

double bonds count as 1 BP

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31
Q

explain how you would deduce the shape of a NH3 molecule

A

central atom is N

N is in group 5 so has 5 outer e-

add an e- for each covalent bond - 5+3 = 8 e-

add e- if you have negative ion, subtract e- if you have positive ion - NH3 is not an ion so ignore this step

divide by two to find number of e- pairs - 8/2 = 4

ne- pairs - ncovalent bonds = nlone pairs

nlone pairs = 4-3 = 1

therefore there are 3BP and 1LP so the shape is trigonal pyramidal

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32
Q

what shape is a XeF2 molecule?

A

linear 180º

2BP and 3LP

basic shape is trigonal bipyramidal but LP repel more than BP so shape takes up this shape to minimise repulsion

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33
Q

give the ideal gas equation and the units

A

pV = nRT

p = pressure in Pa

V = volume in m3 (to convert cm3 to m3 x 10-6, dm3 to m3 x10-3)

n = moles

R = gas constant - 8.31 JK-1mol-1

T = temp in K

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34
Q

electron configuration of Cr and Cu

A

Cr - 1s22s22p63s23p63d54s1

Cu - 1s22s22p63s23p63d104s1

explanation for Cr= one of the 4s2 e- moves to a 3d sub-orbital, this means there is one e- in each orbital of the 3d sub-shell. atom is more stable in this form due to symmetry around nucleus (half-full and full shells more stable)

explanation for Cu - one of the 4s2 e- moves to a 3d sub-orbital. having 10 e- in the 3d sub-shell makes the atom more stable due to the symmetry around the nucleus (full shells are more stable)

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35
Q

what is the electron configuration of a iron(III) ion?

A

iron atoms have 26 e-

4s e- lost first

iron(III) ions have 23 e- , 2e- lost from 4s and 1 e- from the 3d

this gives:

1s22s23s23p63d5

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36
Q

draw the e- configuration of a vanadium atom

A

4s occupied before 3d - because 3d is at a higher energy level than 4s (electrons fill lowest energy sub-shells first)

however still write 3d before 4s

overall e- configruation = 1s22s22p63s23p63d34s2

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37
Q

enthalpy change definition

A

heat energy change at a constant pressure

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38
Q
A

more exothermic

as energy released when water vapour condenses (as making bonds releases energy)

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39
Q

improvements to reduce heat loss in calorimetry experiments

A

reduce distance between flame and beaker

put sleeve around flame to reduce drafts

add lid

use copper calorimeter instead of pyrex beaker

40
Q
A

forward reaction is exothermic

if Kc is larger this means conc of products has increased when temperature was lowered so position of eqm had shifted to the right

41
Q

compare non-polar, polar, and ionic bonds

A
42
Q

The effect of geometric isomerism on physical properties:

A

E isomers have higher melting points because:

E isomers pack together more closely than Z isomers so have stronger intermolecular forces=more energy needed to melt them

Z isomers have higher boiling points because:

  • Z isomers are polar; E isomers are non-polar

When alkyl groups are attached to the C=C bond, they release e- which makes the C atoms in the C=C bond δ+

E isomers still contain polar bonds but overall they are non-polar as the position of the atoms cancel out the δ charges

Z isomers will form permanent dipole-dipole forces as well as VDW forces between molecules which are stronger=more energy required to vaporise

43
Q

describe method to calculate the enthalpy change of neutralisation

A
  • place equal volumes and concs of acid and alkali (at least 1 mol dm-3) in separate beakers
  • allow each to reach equal temps
  • add both acid and alkali to polystyrene cup with lid (to minimise heat loss)
  • record temp at regular intervals until max temp reached
44
Q

write down the half equation for the reduction of NO3- to NO

A
45
Q

define oxidising and reducing agent

A

oxidising agent - accepts e- (so oxidation state decreases) so causes another substance to lose e- thus oxidising it

reducing agent = loses e- (so oxidation state increases) so causes another substance to gain e- thus reducing it

46
Q

write the half equation for the oxidation od SO32- to SO42-

A
47
Q

Why is bond enthalpy measured in the gaseous state only?

A

The gaseous state is the only state in which the intermolecular forces are negligible. We only want to measure the strength of the covalent bonds, so we don’t want any interference of the value from intermolecular forces, which are stronger in solid and liquid state

48
Q

Calculate the ΔfH of CCl4 (l) given the following data:

CCl4 (l) ⟶ CCl4 (g) = +31 kJmol-1

C (s) ⟶ C (g) = +715 kJmol-1

Bond enthalpy (Cl-Cl) = +242 kJmol-1

Bond enthalpy (C-Cl)= +336 kJmol-1

A

First write down the reaction for standard enthalpy of formation of CCl4:

C (s) + 2Cl2 (g) ⟶ CCl4 (l)

Work out the enthalpy change of the reaction using the bond enthalpies. Add on the extra energy needed to convert the C and CCl4 into gaseous state

ΔH= [2(242) – 4(336)] + 31 + 715= -114 kJ mol-1

49
Q

why are iodide ions better reducing agents than chloride ions

A

iodide ions have more energy levels than chloride ions so more shielding

so weaker electrostatic attraction between outermost e- in iodide ions and positive nucleus than in chloride ions

outermost e- more easily removed from iodide ions

50
Q

describe how H bonding occurs

A

occurs when one of the most electronegative atoms (O,F or N) are bonded to Hydrogen

H bonds are the electrostatic attractions between a LP on the electronegative atom (in a molecule) and the δ+ H in another molecule

51
Q

explain the trend in oxidising ability of group 7

A

decreases down group because:

atomic radius and shielding increases = outer e- further from nucleus = weaker electrostatic attraction between outer e- and nucleus

more energy required to gain an e- so atom less likely to be reduced

52
Q

explain the trend in reducing ability of group 7

A

increases down group

ionic radius increases and increased shielding = weaker electrostatic attraction betwen nucleus and outer e- being lost

halide ion more likely to lose an e- because less energy is required to remove it

53
Q

define functional group

A

group of atoms responsible for characteristic reactions of a compound

54
Q

define homologous series

A

group of compounds which :

  • have same general formula
  • differ from successive members by a -CH2 group
  • similar chemical properties
  • show a gradation in physical properties
  • have same functional group
55
Q

define molecular formula

A

actual number of atoms of each element in a compound

56
Q

define displayed formula

A

shows all atoms and all covalent bonds for a compound

ionic bonds are shown using charges

57
Q

define structural formula

A

shows arrangement of atoms in a compound without showing bonds

each carbon is written separately followed by the atoms/groups attached

when groups are attached, a bracket is use to show the group is not part of the main carbon chain

58
Q

define empirical formula

A

simplest whole number ratio of the atoms of each element in a compound

59
Q

define skeletal formula

A

diagrammatic representations of compounds which do not show C or H atoms attached to the carbon chain but do show other atoms (e.g. N,O, and H attached to something other than a C)

60
Q

order these functional groups in decreasing naming priority:

CHO, COCl, CO, COOH, NH2, COO, CN, OH, C=C

A

HIGHEST NAMING PRIORITY:

  • COOH
  • COO
  • COCl
  • CN
  • CHO
  • CO
  • OH
  • NH2
  • C=C

LOWEST NAMING PRIORITY

61
Q

explain why some ionic compounds are soluble in water whereas others are not

A

in most ionic comound, water molecules can knock off ions from the lattice and surround them

in some ionic compounds, the electrostatic attraction between opp charged ions are so high water molecules cannot break up the lattice

ionic substances do not dissolve in non-polar solvents

62
Q

properties of molecular covalent crystals e.g ice and I2

A

low melting points and brittle due to weak VDW forces between molecules

do not conduct electricity as no charged particles

63
Q

diamond - structure and properties

A

macromolecular substance

each C is bonded to 4 others in a tetrahedral arrangement

very high melting pt due to many strong covalent bonds

does not conduct heat/electricity as there are no charged particles that can move

64
Q

graphite structure and properties

A

macromolecular structure

each C atom bonded to 3 others in a hexagonal arrangement with a bond angle of 120º,

layered structure with weak VDW forces between so layers can slide over each other = soft and lubricating

4th e- of each C atom becomes delocalised between layers

high melting point due to many strong covalent bonds between C atoms which require lots of energy to overcome

65
Q

what is the shape and bond angle of SF4 ?

is the molecule polar?

what IMF can be found between its molecules?

A
66
Q

BF3 contains polar bonds but is a non-polar molecule

explain why

A

equally polar bonds are arranged symmetrically around the B atom so the polarities of the bonds cancel out

67
Q

explain how VDW forces arise

A

e- orbiting the nuclei of atoms are in constant rapid motion and at any time they may be distributed more on one side of the molecule than another

this creates a temporary induced dipole

adjacent molecule attracted to the first molecule, inducing a temporary dipole in the next molecule and so on

induced dipoles are continuously forming and disappearing

68
Q

explain trend in electronegativity down a group

A

decreases beause :

atomic radius/shielding increases = weaker attraction between BP of e- and nucleus

69
Q

what does polarity mean?

A

unequal distribution of the e- density in a covalent bond

polar covalent bonds are described as having ionic character so can conduct electricity

70
Q

explain how permanent dipole-dipole forces arise

A

occur betwen polar molecules with permanent dipoles

e- density in covalent bond pulled towards more electronegative atom, 1 atom is delta - the other deta + (known as permanent dipole)

the delta positive end of one molecule attracts the delta negative end of the dipole of another molecule

71
Q

rules for determining oxidation state

A

O is -2 except in peroxides it is -1 (e.g H2O2, K2O2, Na2O2) and if OF2 it is +2

H is +1 except for hydrides it is -1

in simple compounds containing 2 elements, the more electronegative element has the negative oxidation state

72
Q

deduce why the bonding in nitrogen oxide is covalent rather than ionic

A

small electronegativity difference between N and O as both non-metals

73
Q

2A + B ⇌ 3C + D

justify the statement that adding more water to the eqm mixture will lower the amount of A in the mixture [3]

A

[A], [B], [C] and [D] all decrease

pos of eqm shifts to right as more moles on right

so [C] & [D] increase and [A] decreases

74
Q

define addition reaction

A

when a molecule is added to an unsaturated compound to form a saturated compound

75
Q

state the observations you can make when:

a) Mg reacts with steam [2]
b) Na is heated with oxygen [2]

A

a)white solid

bright white flame

b)white solid

yellow flame

76
Q

By reference to the structure of, and the bonding in, silicon dioxide, suggest why it is insoluble in water.

A

macromolecular with covalent bonding

water cannot supply enough energy to break strong covalent bonds

77
Q

Some Period 3 oxides have basic properties. State the type of bonding in these basic oxides. Explain why this type of bonding causes these oxides to have basic properties

A

ionic bonding

contain O2- ions which accept H+ from water to form OH- ions

78
Q

Suggest why silicon dioxide is described as an acidic oxide even though it is insoluble in water.[1]

A

it reacts with bases

79
Q

flame tests

A

Na+ = yellow flame

Ca2+ = Brick red

Sr2+ = Red

Ba2+ = Pale green

80
Q

why does the bpt of haloalkanes increase down group 7?

A

if number of carbons increases and/or X atom gets bigger :

bigger Mr so more e- = stronger VDW forces

if same number of carbons look at electronegativity of X atom

higher electronegativity = higher polarity of C-X bond = stronger VDW forces

81
Q

what has higher naming priority, alkene or haloalkane group?

A

alkene group

82
Q

solubility of haloalkanes

A

insoluble in water

although CX bond is polar, large R group gets in way of H bond formation with water

83
Q

there are 3 separate solid samples. 1 is sodium carbonate, another is sodium fluoride and the last is sodium chloride

outline a logical sequence of test-tube reactions to identify each compound

include observations and equations with state symbols for any reactions

[6]

A
  • dissolve each solid in same volume of water in separate test tubes
  • add HNO3 to each solution (used as nitrate ions never form ppts)
  • test tube with sodium carbonate would show effervescence
    • Na2CO3(s) + 2HNO3 → 2NaNO3 (aq) + CO2(g) +H2O(l)
  • add AgNO3 (aq) to the other two test tubes
  • no visible change for test tube with sodium fluoride
  • test tube with sodium chloride forms white ppt
    • Cl-(aq) + Ag+ (aq) → AgCl(s)
84
Q

what causes geometrical isomerism to occur? [2]

A

restricted rotation around C=C bond

different priority groups attached to the 2 C of the C=C bond

85
Q

why are secondary carbocations less stable than tertiary carbocations ?

A

3º carbocations have 3 R groups attached directly to the positive C atoms

2º carbocations have 2 R groups directly attached to the positive C atom

therefore 2º carbocations have a weaker positive inductive effect ( the e- density is less repelled toward the positive C atoms so the C+ is less stabilised)

86
Q

in the test for halide ions,

dilute nitric acid is added before silver nitrate solution

explain why [1]

A

to prevent precipitation of silver compounds other than halides

87
Q

which of these period 3 elements has the highest first IE?

A : Al

B: P

C: Si

D: S

A

correct answer : B (Phosphorus)

increasing first IE across period but S is an exception

first IE of S lower than first IE of P due to 3p4 configuration

88
Q

which of these elements has the highest second IE?

A: Na

B: Mg

C: Ne

D: Ar

A

correct answer: A

Na outer electron is in 3s orbital

Na+ outer electron removed from full 2 shell

as changing from 3rd energy level to 2nd energy level (all other e- have their second e- removed from the shame shell as first e-) large amount of energy required

89
Q

which period 3 element has the highest melting point

A: Al

B: P

C: Na

D: S

A

answer: A

as Al has metallic bonding

metallic bonding in Al stronger than in Na

P4 and S8 has simple molecular structure with weak VDW forces so lower melting points

90
Q

which elements are shown in increasing order of the stated property:

A: atomic radius : Phosphorus, Sulfur, Sodium

B: first IE : Sodium, Magnesium, Aluminium

C: electronegativity : Sulfur, Phosphorus, Silicon

D: melting point : Argon , chlorine, sulfur

A

correct answer: D

B incorrect as Al has lower first IE than Mg

91
Q

define elimination reaction

A

when a molecule lost from saturated compound to form an unsaturated compound

A → B + C

92
Q

define substitution reaction

A

when an atom/group replaces another atom/group

AB + CD → AD + BC

93
Q

a) Acid + metal→ ?
b) acid + metal oxide →
c) acid + metal/hydrogencarbonate →
d) acid + ammonia →
e) metal + water →
f) metal carbonate (when heated) →

A

a) salt + hydrogen
b) salt + water
c) salt + water + carbon dioxide
d) ammonium salt
e) metal hydroxide + hydrogen gas
f) metal + carbon dioxide (thermal decomposition)

94
Q

chlorine reacts with cold aqueous NaOH in the manufacture of bleach

give the reaction

A

Cl2 +2NaOH → NaCl + NaClO + H2O

95
Q

reaction of halides with sulfuric acid e.g NaCl + H2SO4

A

NaCl + H2SO4 → HCl + NaHSO4

hydrogen halide + hydrogen sulfate salt

sulfuric acid acts as an oxidising agent