<s>[INST] You are a smart text analyzer assistant.
Given a QUESTION and a set of posible texts from which to derive the answer, examine each text and reply whether or not the ANSWER exists within the text.
You MUST give the response in a VALID JSON object with a Yes or No for each text.


So for instance the following:

QUESTION: What is the color of the sky?
POSIBLE ANSWERS:
Source 1: The sky is blue
Source 2: The sea is blue
Source 3: The sky is blue in the daytime but black at night

would give an output of:[/INST]

{
"Source 1": "Yes",
"Source 2": "No",
"Source 3": "Yes"
}
</s>
 
[INST]
QUESTION: how to get from alcohol to alkyl halide
POSIBLE ANSWERS:
Source 1: To summarize, since alcohols can be made into alkyl halides and can also be made into aldehydes and ketones, they are important starting points for carrying out a Grignard synthesis. As products of Grignard syntheses, they are also useful materials to begin a new cycle. Since the product here is a secondary alcohol, the scheme could be carried onwards through its oxidation to a ketone and/or its conversion to an alkyl bromide, etc.
Source 2: The alcohol product of this sequence can be used to make an alkyl halide to start a new sequence, which could be the starting point for a further sequence, etc. This makes alcohols extremely valuable synthetic reagents. Since the product here is a secondary alcohol, the scheme could be carried onwards through its oxidation to a ketone and/or its conversion to an alkyl bromide, etc.
Source 3: Reaction type: Nucleophilic Substitution (SN1 or SN2). Summary: 1  When treated with HBr or HCl alcohols typically undergo a nucleophilic substitution reaction to generate an alkyl halide and water. Reaction of Alcohols with other Halogenating agents (SOCl2, PX3). Reaction type: Nucleophilic Substitution (SN1 or SN2). Summary: 1  Alcohols can also be converted to alkyl chlorides using thionyl chloride, SOCl2, or phosphorous trichloride, PCl3. 2  Alkyl bromides can be prepared in a similar reaction using PBr3. 3  Used mostly for 1o and 2o ROH. 4  In each case a base is used to mop-up the acidic by-product
[/INST]
<s>[INST] You are a smart text analyzer assistant.
Given a QUESTION and a set of posible texts from which to derive the answer, examine each text and reply whether or not the ANSWER exists within the text.
You MUST give the response in a VALID JSON object with a Yes or No for each text.


So for instance the following:

QUESTION: What is the color of the sky?
POSIBLE ANSWERS:
Source 1: The sky is blue
Source 2: The sea is blue
Source 3: The sky is blue in the daytime but black at night

would give an output of:[/INST]

{
"Source 1": "Yes",
"Source 2": "No",
"Source 3": "Yes"
}
</s>
 
[INST]
QUESTION: how to get from alcohol to alkyl halide
POSIBLE ANSWERS:
Source 1: To summarize, since alcohols can be made into alkyl halides and can also be made into aldehydes and ketones, they are important starting points for carrying out a Grignard synthesis. As products of Grignard syntheses, they are also useful materials to begin a new cycle. Since the product here is a secondary alcohol, the scheme could be carried onwards through its oxidation to a ketone and/or its conversion to an alkyl bromide, etc.
Source 2: The alcohol product of this sequence can be used to make an alkyl halide to start a new sequence, which could be the starting point for a further sequence, etc. This makes alcohols extremely valuable synthetic reagents. Since the product here is a secondary alcohol, the scheme could be carried onwards through its oxidation to a ketone and/or its conversion to an alkyl bromide, etc.
Source 3: Reaction type: Nucleophilic Substitution (SN1 or SN2). Summary: 1  When treated with HBr or HCl alcohols typically undergo a nucleophilic substitution reaction to generate an alkyl halide and water. Reaction of Alcohols with other Halogenating agents (SOCl2, PX3). Reaction type: Nucleophilic Substitution (SN1 or SN2). Summary: 1  Alcohols can also be converted to alkyl chlorides using thionyl chloride, SOCl2, or phosphorous trichloride, PCl3. 2  Alkyl bromides can be prepared in a similar reaction using PBr3. 3  Used mostly for 1o and 2o ROH. 4  In each case a base is used to mop-up the acidic by-product
[/INST]
{
"Source 1": "Yes",
"Source 2": "Yes",
"Source 3": "Yes"
}
<s>[INST] You are a smart text analyzer assistant.
Given a QUESTION and a set of posible texts from which to derive the answer, examine each text and reply whether or not the ANSWER exists within the text.
You MUST give the response in a VALID JSON object with a Yes or No for each text.


So for instance the following:

QUESTION: What is the color of the sky?
POSIBLE ANSWERS:
Source 1: The sky is blue
Source 2: The sea is blue
Source 3: The sky is blue in the daytime but black at night

would give an output of:[/INST]

{
"Source 1": "Yes",
"Source 2": "No",
"Source 3": "Yes"
}
</s>
 
[INST]
QUESTION: how to get from alcohol to alkyl halide
POSIBLE ANSWERS:
Source 1: To summarize, since alcohols can be made into alkyl halides and can also be made into aldehydes and ketones, they are important starting points for carrying out a Grignard synthesis. As products of Grignard syntheses, they are also useful materials to begin a new cycle. Since the product here is a secondary alcohol, the scheme could be carried onwards through its oxidation to a ketone and/or its conversion to an alkyl bromide, etc.
Source 2: The alcohol product of this sequence can be used to make an alkyl halide to start a new sequence, which could be the starting point for a further sequence, etc. This makes alcohols extremely valuable synthetic reagents. Since the product here is a secondary alcohol, the scheme could be carried onwards through its oxidation to a ketone and/or its conversion to an alkyl bromide, etc.
Source 3: Reaction type: Nucleophilic Substitution (SN1 or SN2). Summary: 1  When treated with HBr or HCl alcohols typically undergo a nucleophilic substitution reaction to generate an alkyl halide and water. Reaction of Alcohols with other Halogenating agents (SOCl2, PX3). Reaction type: Nucleophilic Substitution (SN1 or SN2). Summary: 1  Alcohols can also be converted to alkyl chlorides using thionyl chloride, SOCl2, or phosphorous trichloride, PCl3. 2  Alkyl bromides can be prepared in a similar reaction using PBr3. 3  Used mostly for 1o and 2o ROH. 4  In each case a base is used to mop-up the acidic by-product
[/INST]
{
"Source 1": "No",
"Source 2": "No",
"Source 3": "No"
}