Alkanes Flashcards

1
Q

What’s syn addition ?

A

If during addition reaction of an alkene the groups are attached on the same side it’s called syn addition.

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2
Q

What’s anti addition ?

A

If during addition reaction the groups are attached on the opposite direction then the addition is called anti addition.

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3
Q

In case of catalytic addition of H2 what kind of addition takes place ?

A

Syn addition

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4
Q

If the Alkane is unsymmetrical , then it forms what kind of mixture in addition ?

A

Racemic mixture , irrespective of syn or anti.

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5
Q

What does Red phosphorous and HI do when they act as catalyst to alchols and compounds containing C=O ?

A

Red phosphorus and HI reduces them to Alkane

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6
Q

With 1 degree halide , LiAlH4 reacts with which mechanism to form Alkane? What about NaBH4?

A

With 1 degree halide , LiAlH4 reacts in SN2 mechanism to form Alkane and NaBH4 does not undergo any reaction.

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7
Q

With 2 degree alkyl halide , LiAlH4 reacts with which mechanism to form Alkane? What about NaBH4?

A

LiAlH4 undergoes SN2 mechanism whereas NaBH4 undergoes SN1 mechanism through carbocation formation of hallide.

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8
Q

With 3 alkyl degree halide , LiAlH4 reacts with which mechanism to form Alkane? What about NaBH4?

A

LiBH4 will act as a base with 3 degree hallide through elimination reaction whereas NaBH4 will proceed through SN1 mechanism.

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9
Q

Catalytic Hydrogenation Reaction of Alkenes

A

CH3-CH=CH2–(H2,Pt/Pd/Ni)–> CH3-CH2-CH2.

Energy released during chemisorption is more than energy to break H-H bonds.

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10
Q

Sabatier Sandern’s reaction CnH2n—>?

A

CnH2n/CnH2n-2—H2,Ni/573K——->CnH2n+2

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11
Q

Alkane preparation by alkene reduction

A

(CH₃)₂-C=CH₂—Pd-C/C₂H₅OH—> (CH₃)₂CHCH₃

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12
Q

Alkane preparation by alkyl halide reduction

A

RX + H2–RA–>RH + HX
; X = Halogen
RA= Zn + CH3COOH/ Zn+ HCl

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13
Q

Wurtz Reaction for alkanes

A

2RI+Na–dry ether–>R-R+NaI

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14
Q

Alkane preparation by alkyl iodide reduction

A

RI+HI–Red Phosphorous/150 C–>RH-I2

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15
Q

Frankland Reaction ( Alkanes )

A

RI+Zn+RI—->RR+ZnI2

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16
Q

Alkane preparation by alcohol reduction

A

ROH+2HI–Red Phosphorous,150 C–>RH+I2+H2O

17
Q

Clemmension’s Reaction for Alkanes

A

RCHO+2H2–(Zn-Hg),HCl–>RCH3+ H20

18
Q

Alkane preparation by carboxylic acid reduction

A

RCOOH+6HI–Red Phosphorous–>RCH3+2H20+3I2

19
Q

Decarboxylation reaction ( Alkane )

A

RCOONa+ NaOH–CaO,heat–>RH+ Na2CO3

20
Q

Kolbe’s Electrolysis ( Alkanes )

A

2CH3COONa+ H20–electrolysis–>CH3-CH3+ CO2 + 2NaOH + H2
; At anode = CH3-CH3+CO2
At cathode = H2

21
Q

Alkane preparation by Aluminium Carbide

A

Al₄C₃+12H₂0—->3CH₄+4Al(OH)₃

22
Q

Alkane preparation by beryllium carbide

A

Be2C+H20—->CH4+2Be(OH)2

23
Q

Corey House Synthesis

A

RX+2Li–diethyl ether–>RLi+LiX–diethyl ether–R2CuLi+LiI—->R-R’+RCu+LiX

24
Q

Swartz Reaction (Alkanes)

A

2CH₃CH₂-Cl+Hg₂F₂—->2CH₃CH₂F+Hg₂Cl₂

25
Q

Halogenation of Alkane

A

CH4–Cl2/hv–>CH3Cl–Cl2/hv–>CH2Cl2–Cl2/hv–>CH3Cl–Cl/hv–>CCl4

26
Q

Order of ease of Halogenation

A

3⁰RX->2⁰RX->1⁰RX->CH₄