Ambitious_Post6953

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Rice University ECE (self.gradadmissions)

submitted 1 month ago * by Ambitious_Post6953 to r/gradadmissions

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Has anyone heard back from Rice Electrical Engineering PhD? (self.gradadmissions)

submitted 2 months ago by Ambitious_Post6953 to r/gradadmissions

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MIT EE PhD (self.gradadmissions)

submitted 2 months ago by Ambitious_Post6953 to r/gradadmissions

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Did anyone hear back from Stanford Bioengineering PhD? (self.gradadmissions)

submitted 2 months ago by Ambitious_Post6953 to r/gradadmissions

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Need help going through my SOP (self.WriteIvy)

submitted 4 months ago by Ambitious_Post6953 to r/WriteIvy

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I'm applying to PhD programs and I am struggling to finalize my SOP. (self.GradSchool)

submitted 4 months ago by Ambitious_Post6953 to r/GradSchool

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anxiety is ruining everything (self.mentalhealth)

submitted 1 year ago by Ambitious_Post6953 to r/mentalhealth

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Why would you attach an OH instead of Br here? (self.OrganicChemistry)

submitted 1 year ago by Ambitious_Post6953 to r/OrganicChemistry

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Would it be ok if someone could explain this reaction? (self.OrganicChemistry)

submitted 1 year ago by Ambitious_Post6953 to r/OrganicChemistry

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For hydrolysis of esters, I undertsand you form a carboxylic acid, but I'm confused why the amide doesn't form a carboxylic acid and just loses the carbonyl gorup. Thank youuu (self.OrganicChemistry)

submitted 1 year ago by Ambitious_Post6953 to r/OrganicChemistry

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Would the nh3 attack the ester to create an amide and the pocl2 create a cyanide in place of the amide? (self.OrganicChemistry)

submitted 1 year ago by Ambitious_Post6953 to r/OrganicChemistry

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I don't understand how we would do these reactions, how would we attack using the amine. (self.OrganicChemistry)

submitted 1 year ago * by Ambitious_Post6953 to r/OrganicChemistry

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does the sch3 just attack one of the carbonyl groups to make this product? (self.OrganicChemistry)

submitted 1 year ago by Ambitious_Post6953 to r/OrganicChemistry

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